NO813354L - Bis(substituerte fenyl)alkyltinn-forbindelser - Google Patents

Bis(substituerte fenyl)alkyltinn-forbindelser

Info

Publication number: NO813354L
Authority: NO; Norway
Prior art keywords: halogen; sup; composition; compounds; stated
Prior art date: 1980-10-08

Application number

NO813354A

Other languages

English (en)

Norwegian (no)

Inventor

Melvin Hyman Gitlitz

David Alan Russo

Original Assignee

M & T Chemicals Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1980-10-08

Filing date

1981-10-02

Publication date

1982-04-13

1981-10-02 Application filed by M & T Chemicals Inc filed Critical M & T Chemicals Inc

1982-04-13 Publication of NO813354L publication Critical patent/NO813354L/no

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 83
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 title description 4
125000000217 alkyl group Chemical group 0.000 claims abstract description 35
229910052736 halogen Inorganic materials 0.000 claims abstract description 30
150000002367 halogens Chemical group 0.000 claims abstract description 30
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 16
125000002947 alkylene group Chemical group 0.000 claims abstract description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 10
125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
239000000417 fungicide Substances 0.000 claims abstract description 9
125000003118 aryl group Chemical group 0.000 claims abstract description 7
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
239000001301 oxygen Substances 0.000 claims abstract description 6
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims abstract description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 5
239000005864 Sulphur Substances 0.000 claims abstract description 4
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims abstract description 4
239000012990 dithiocarbamate Substances 0.000 claims abstract description 4
125000004953 trihalomethyl group Chemical group 0.000 claims abstract description 4
125000005309 thioalkoxy group Chemical group 0.000 claims abstract 4
239000000203 mixture Substances 0.000 claims description 34
239000000460 chlorine Substances 0.000 claims description 19
229910052801 chlorine Inorganic materials 0.000 claims description 19
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
230000000855 fungicidal effect Effects 0.000 claims description 10
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 9
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 9
229910052794 bromium Inorganic materials 0.000 claims description 9
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
230000012010 growth Effects 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
230000002538 fungal effect Effects 0.000 claims description 3
125000004001 thioalkyl group Chemical group 0.000 claims description 3
125000001246 bromo group Chemical group Br* 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
-1 methylsulphonyl Chemical group 0.000 abstract description 19
101100379079 Emericella variicolor andA gene Proteins 0.000 abstract 1
231100000674 Phytotoxicity Toxicity 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 27
239000000243 solution Substances 0.000 description 23
238000002360 preparation method Methods 0.000 description 19
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 15
229910052718 tin Inorganic materials 0.000 description 15
241000196324 Embryophyta Species 0.000 description 14
238000000034 method Methods 0.000 description 14
239000000047 product Substances 0.000 description 14
239000000758 substrate Substances 0.000 description 13
241000233866 Fungi Species 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
239000002904 solvent Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000007787 solid Substances 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
239000000463 material Substances 0.000 description 8
125000001424 substituent group Chemical group 0.000 description 8
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 8
241000221785 Erysiphales Species 0.000 description 7
239000007788 liquid Substances 0.000 description 7
238000003359 percent control normalization Methods 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
240000006365 Vitis vinifera Species 0.000 description 6
235000014787 Vitis vinifera Nutrition 0.000 description 6
239000006227 byproduct Substances 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
239000007983 Tris buffer Substances 0.000 description 5
235000009754 Vitis X bourquina Nutrition 0.000 description 5
235000012333 Vitis X labruscana Nutrition 0.000 description 5
125000002877 alkyl aryl group Chemical group 0.000 description 5
125000000129 anionic group Chemical group 0.000 description 5
125000003710 aryl alkyl group Chemical group 0.000 description 5
239000003921 oil Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000002253 acid Substances 0.000 description 4
238000009835 boiling Methods 0.000 description 4
238000003776 cleavage reaction Methods 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
238000001914 filtration Methods 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 3
MXOAEAUPQDYUQM-UHFFFAOYSA-N chlorphenesin Chemical compound OCC(O)COC1=CC=C(Cl)C=C1 MXOAEAUPQDYUQM-UHFFFAOYSA-N 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
201000010099 disease Diseases 0.000 description 3
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 3
150000004820 halides Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
230000007017 scission Effects 0.000 description 3
239000007921 spray Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000002023 wood Substances 0.000 description 3
XKNHJNPWITUSBZ-UHFFFAOYSA-K 4,4-bis(4-chlorophenyl)butyl-tribromostannane Chemical compound C1=CC(Cl)=CC=C1C(CCC[Sn](Br)(Br)Br)C1=CC=C(Cl)C=C1 XKNHJNPWITUSBZ-UHFFFAOYSA-K 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
229940126062 Compound A Drugs 0.000 description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
241001281803 Plasmopara viticola Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
YHFNAWGMSOHMLB-UHFFFAOYSA-K benzhydryltin(3+);trichloride Chemical compound [Cl-].[Cl-].[Cl-].C=1C=CC=CC=1C([Sn+3])C1=CC=CC=C1 YHFNAWGMSOHMLB-UHFFFAOYSA-K 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
FAOSYNUKPVJLNZ-UHFFFAOYSA-N butylstannane Chemical compound CCCC[SnH3] FAOSYNUKPVJLNZ-UHFFFAOYSA-N 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 2
239000007789 gas Substances 0.000 description 2
238000007429 general method Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
150000008282 halocarbons Chemical class 0.000 description 2
239000012433 hydrogen halide Substances 0.000 description 2
229910000039 hydrogen halide Inorganic materials 0.000 description 2
239000000976 ink Substances 0.000 description 2
238000011081 inoculation Methods 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
239000003973 paint Substances 0.000 description 2
239000000123 paper Substances 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
238000010992 reflux Methods 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
125000003944 tolyl group Chemical group 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
HVKCZUVMQPUWSX-UHFFFAOYSA-N 1-bromo-2,3-dichlorobenzene Chemical compound ClC1=CC=CC(Br)=C1Cl HVKCZUVMQPUWSX-UHFFFAOYSA-N 0.000 description 1
NHDODQWIKUYWMW-UHFFFAOYSA-N 1-bromo-4-chlorobenzene Chemical compound ClC1=CC=C(Br)C=C1 NHDODQWIKUYWMW-UHFFFAOYSA-N 0.000 description 1
125000005916 2-methylpentyl group Chemical group 0.000 description 1
125000003469 3-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
JTQBSBRTEHKOQK-UHFFFAOYSA-N 4,4,4-tris(4-chlorophenyl)butyltin Chemical compound C1=CC(Cl)=CC=C1C(CCC[Sn])(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 JTQBSBRTEHKOQK-UHFFFAOYSA-N 0.000 description 1
KXEOAJCDHTWQOI-UHFFFAOYSA-K 4,4-bis(4-chlorophenyl)butyltin(3+);trihydroxide Chemical compound [OH-].[OH-].[OH-].C1=CC(Cl)=CC=C1C(CCC[Sn+3])C1=CC=C(Cl)C=C1 KXEOAJCDHTWQOI-UHFFFAOYSA-K 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
XPAOTXKQYDDKRI-UHFFFAOYSA-K CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.C1=CC(Cl)=CC=C1C(CCC[Sn+3])C1=CC=C(Cl)C=C1 Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.C1=CC(Cl)=CC=C1C(CCC[Sn+3])C1=CC=C(Cl)C=C1 XPAOTXKQYDDKRI-UHFFFAOYSA-K 0.000 description 1
101100491149 Caenorhabditis elegans lem-3 gene Proteins 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
239000005747 Chlorothalonil Substances 0.000 description 1
239000004338 Dichlorodifluoromethane Substances 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
QCQYNYWXPHCAAZ-UHFFFAOYSA-M [Cl-].[Mg+]C1=CC=C(Cl)C=C1 Chemical compound [Cl-].[Mg+]C1=CC=C(Cl)C=C1 QCQYNYWXPHCAAZ-UHFFFAOYSA-M 0.000 description 1
FXMSAEZOCGPHTO-UHFFFAOYSA-M [butyl-bis(4-chlorophenyl)stannyl] 4-methylbenzenesulfonate Chemical compound C=1C=C(Cl)C=CC=1[Sn](C=1C=CC(Cl)=CC=1)(CCCC)OS(=O)(=O)C1=CC=C(C)C=C1 FXMSAEZOCGPHTO-UHFFFAOYSA-M 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
ZQRHOGSBQCDNQR-UHFFFAOYSA-N benzhydryltin Chemical compound C=1C=CC=CC=1C([Sn])C1=CC=CC=C1 ZQRHOGSBQCDNQR-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
230000002051 biphasic effect Effects 0.000 description 1
XWNRCCHVPFIXMA-UHFFFAOYSA-M bis(3,4-dichlorophenyl)-methylstannanylium;acetate Chemical compound C=1C=C(Cl)C(Cl)=CC=1[Sn](C)(OC(=O)C)C1=CC=C(Cl)C(Cl)=C1 XWNRCCHVPFIXMA-UHFFFAOYSA-M 0.000 description 1
RAQQQRJYOBWRDN-UHFFFAOYSA-K bis(4-bromophenyl)methyltin(3+);triacetate Chemical compound CC([O-])=O.CC([O-])=O.CC([O-])=O.C1=CC(Br)=CC=C1C([Sn+3])C1=CC=C(Br)C=C1 RAQQQRJYOBWRDN-UHFFFAOYSA-K 0.000 description 1
ORGGICFXDOFWGU-UHFFFAOYSA-N bis(4-chlorophenyl)methyl-sulfanylidenetin Chemical compound C1=CC(Cl)=CC=C1C([Sn]=S)C1=CC=C(Cl)C=C1 ORGGICFXDOFWGU-UHFFFAOYSA-N 0.000 description 1
LEGGZGGFUGNBLT-UHFFFAOYSA-K bis(4-chlorophenyl)methyltin(3+);trihydroxide Chemical compound [OH-].[OH-].[OH-].C1=CC(Cl)=CC=C1C([Sn+3])C1=CC=C(Cl)C=C1 LEGGZGGFUGNBLT-UHFFFAOYSA-K 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
YMLFYGFCXGNERH-UHFFFAOYSA-K butyltin trichloride Chemical compound CCCC[Sn](Cl)(Cl)Cl YMLFYGFCXGNERH-UHFFFAOYSA-K 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000000969 carrier Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000010730 cutting oil Substances 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003599 detergent Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
ISXUHJXWYNONDI-UHFFFAOYSA-L dichloro(diphenyl)stannane Chemical compound C=1C=CC=CC=1[Sn](Cl)(Cl)C1=CC=CC=C1 ISXUHJXWYNONDI-UHFFFAOYSA-L 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
AWYFNIZYMPNGAI-UHFFFAOYSA-N ethylenebis(dithiocarbamic acid) Chemical compound SC(=S)NCCNC(S)=S AWYFNIZYMPNGAI-UHFFFAOYSA-N 0.000 description 1
238000012854 evaluation process Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
230000002015 leaf growth Effects 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
239000011968 lewis acid catalyst Substances 0.000 description 1
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
229920000940 maneb Polymers 0.000 description 1
150000002696 manganese Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
229920002113 octoxynol Polymers 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000012071 phase Substances 0.000 description 1
125000005561 phenanthryl group Chemical group 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000003822 preparative gas chromatography Methods 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000012360 testing method Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
BYQWEYFCJKJRHO-UHFFFAOYSA-K tribromo(butyl)stannane Chemical compound CCCC[Sn](Br)(Br)Br BYQWEYFCJKJRHO-UHFFFAOYSA-K 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
SKLQBHROODDCHR-UHFFFAOYSA-N trityltin Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)([Sn])C1=CC=CC=C1 SKLQBHROODDCHR-UHFFFAOYSA-N 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
- A01N55/04—Tin
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/226—Compounds with one or more Sn-S linkages

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Confectionery (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyesters Or Polycarbonates (AREA)

NO813354A 1980-10-08 1981-10-02 Bis(substituerte fenyl)alkyltinn-forbindelser NO813354L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/195,276 US4324798A (en)	1980-10-08	1980-10-08	Fungicidal bis(substituted phenyl)alkyltin compounds

Publications (1)

Publication Number	Publication Date
NO813354L true NO813354L (no)	1982-04-13

Family

ID=22720771

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO813354A NO813354L (no)	1980-10-08	1981-10-02	Bis(substituerte fenyl)alkyltinn-forbindelser

Country Status (14)

Country	Link
US (1)	US4324798A (es)
EP (1)	EP0049643B1 (es)
JP (1)	JPS5793990A (es)
AT (1)	ATE14315T1 (es)
AU (1)	AU540569B2 (es)
BR (1)	BR8106485A (es)
CA (1)	CA1164883A (es)
DE (1)	DE3171410D1 (es)
DK (1)	DK444781A (es)
ES (1)	ES506083A0 (es)
IL (1)	IL63906A (es)
MX (1)	MX6992E (es)
NO (1)	NO813354L (es)
ZA (1)	ZA816949B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2113093B (en) *	1982-01-19	1985-01-03	Dow Chemical Co	Improvements in pesticidal formulations
TR22508A (tr) *	1983-02-08	1987-09-19	Dow Chemical Co	Biyolojik aktiviteye sahip suebstitueentli kalay bilesiklerinin tuerevleri,soezkonusu tuerevlerin emuelsifiye edilebilir konsantreler ive bitkilerin zararhlarla istila edilmesini kontrol etmek icin yoentemler
AR243195A1 (es) *	1985-09-03	1993-07-30	Shionogi & Co Ltd Y Nitto Kase	Compuestos de tri-organo-estano y composiciones pesticidas que los contienen
KR900003409B1 (ko) *	1988-05-14	1990-05-18	한국과학기술원	β-알콕시카르보닐에틸주석 디티오카르바메이트 유도체 및 그 제조방법
JP4020130B2 (ja)	2005-06-08	2007-12-12	ヤマハ株式会社	ドラム用フットペダル

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3031483A (en) *	1957-11-18	1962-04-24	Philips Corp	Method of producing organic tin compounds and preparations containing such compoundsfor combating noxious micro-organisms
DE1161076B (de) *	1960-08-30	1964-01-09	Bayer Ag	Verfahren zum Schutz von keratinhaltigem Material gegen Schaedlinge
DE1214237B (de) *	1964-07-10	1966-04-14	Studiengesellschaft Kohle Mbh	Verfahren zur Herstellung von halogenhaltigen Organozinnverbindungen
US3475473A (en) *	1966-10-11	1969-10-28	Nitto Kasei Co Ltd	Process for preparing triorganotin halides and bis(triorganotin) oxides
US3471539A (en) *	1967-08-23	1969-10-07	Nitto Kasei Co Ltd	Method for preparing triorganotin halides and bis(triorganotin) oxides
US3475472A (en) *	1967-09-21	1969-10-28	Nitto Kasei Co Ltd	Method for preparing triorganotin halides and bis(triorganotin) oxides
GB1232691A (es) *	1968-04-25	1971-05-19
NL6805920A (es) *	1968-04-25	1969-10-28
NL7600555A (nl)	1975-03-06	1976-09-08	Ciba Geigy	Werkwijze voor het bereiden van triorganotinha- logeniden en de toepassing daarvan.

1980
- 1980-10-08 US US06/195,276 patent/US4324798A/en not_active Expired - Lifetime
1981
- 1981-09-22 IL IL63906A patent/IL63906A/xx unknown
- 1981-10-02 NO NO813354A patent/NO813354L/no unknown
- 1981-10-06 MX MX819700U patent/MX6992E/es unknown
- 1981-10-07 AU AU76111/81A patent/AU540569B2/en not_active Ceased
- 1981-10-07 ZA ZA816949A patent/ZA816949B/xx unknown
- 1981-10-07 DK DK444781A patent/DK444781A/da not_active Application Discontinuation
- 1981-10-07 ES ES506083A patent/ES506083A0/es active Granted
- 1981-10-07 BR BR8106485A patent/BR8106485A/pt unknown
- 1981-10-07 CA CA000387473A patent/CA1164883A/en not_active Expired
- 1981-10-08 JP JP56159556A patent/JPS5793990A/ja active Pending
- 1981-10-08 EP EP81304669A patent/EP0049643B1/en not_active Expired
- 1981-10-08 AT AT81304669T patent/ATE14315T1/de not_active IP Right Cessation
- 1981-10-08 DE DE8181304669T patent/DE3171410D1/de not_active Expired

Also Published As

Publication number	Publication date
ES8206540A1 (es)	1982-08-16
ATE14315T1 (de)	1985-08-15
AU7611181A (en)	1982-04-22
IL63906A (en)	1985-12-31
ZA816949B (en)	1982-10-27
ES506083A0 (es)	1982-08-16
CA1164883A (en)	1984-04-03
BR8106485A (pt)	1982-06-22
MX6992E (es)	1987-01-26
JPS5793990A (en)	1982-06-11
DK444781A (da)	1982-04-09
AU540569B2 (en)	1984-11-22
EP0049643B1 (en)	1985-07-17
DE3171410D1 (en)	1985-08-22
US4324798A (en)	1982-04-13
EP0049643A3 (en)	1982-06-23
IL63906A0 (en)	1981-12-31
EP0049643A2 (en)	1982-04-14

Publication	Publication Date	Title
NO141340B (no)	1979-11-12	Anilider for anvendelse som mikrobicider
US3856814A (en)	1974-12-24	Olan-2-ylidenemalonates
NO813354L (no)	1982-04-13	Bis(substituerte fenyl)alkyltinn-forbindelser
US3789057A (en)	1974-01-29	A process for preparing symetrical triorganotin halides
US2767114A (en)	1956-10-16	Seed disinfectants containing arsenate salts of monothio acids
US2839446A (en)	1958-06-17	New pyrimidine derivatives
US3784580A (en)	1974-01-08	Organosulfonylmethyl(trihydrocarbyl)tin compounds
EP0102163B1 (en)	1987-04-01	Triazole derivatives and compositions containing the same
KR920002887B1 (ko)	1992-04-06	오르가노틴 화합물의 제조방법
US3850970A (en)	1974-11-26	Novel organotin compounds
US3140226A (en)	1964-07-07	Microorganism toxic alpha-chloro-betacyanoethylaryl sulfones
US2988475A (en)	1961-06-13	Fungicide
DE2114367B2 (de)	1979-03-22	Organische Zinnverbindungen und deren Verwendung als Herbizide
US4191698A (en)	1980-03-04	Tricyclopentyltin fluoride
CA1058193A (en)	1979-07-10	1,3-dithiol-2-ylidene malonic esters, process for preparing the same, and use of said esters
US3790611A (en)	1974-02-05	Tris(cyclohexylalkyl)tin or hexakis(cyclohexylalkyl)tin compounds
US3709960A (en)	1973-01-09	O-loweralkyl-o-(2-alkoxylcarbonylmethyl)vinyl-monoalkylamido phosphates
US3454611A (en)	1969-07-08	Dialkyltin substituted phthalates
US3595963A (en)	1971-07-27	Method of controlling the growth of fungi
US3346596A (en)	1967-10-10	Tricyclic ketal compounds having biological activity
US4343815A (en)	1982-08-10	Method for combating fungi and mites using certain triorganotin compounds
US3673200A (en)	1972-06-27	3(2-sec-butyl-4,6-dimitrophenoxy)-1,2-benzisothiozole 1,1-dioxide
US3677738A (en)	1972-07-18	Method for the control of pests with triorganotin (substituted phenoxides)
US3798327A (en)	1974-03-19	Fungicidal compositions and their use
US3316264A (en)	1967-04-25	2-phenylthio-4-alkoxy-6-halo-s-triazines