UY26044A1 - HERBICIDALLY ACTIVE PIRIDILSULFONILUREA SALTS - Google Patents
HERBICIDALLY ACTIVE PIRIDILSULFONILUREA SALTSInfo
- Publication number
- UY26044A1 UY26044A1 UY26044A UY26044A UY26044A1 UY 26044 A1 UY26044 A1 UY 26044A1 UY 26044 A UY26044 A UY 26044A UY 26044 A UY26044 A UY 26044A UY 26044 A1 UY26044 A1 UY 26044A1
- Authority
- UY
- Uruguay
- Prior art keywords
- compounds
- salts
- dimethyl
- metolachlor
- dioxane
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 abstract 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 2
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 abstract 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 abstract 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 abstract 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 1
- 239000005499 Clomazone Substances 0.000 abstract 1
- 239000005533 Fluometuron Substances 0.000 abstract 1
- 239000005561 Glufosinate Substances 0.000 abstract 1
- 239000005562 Glyphosate Substances 0.000 abstract 1
- LXKOADMMGWXPJQ-UHFFFAOYSA-N Halosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C(O)=O)C)=N1 LXKOADMMGWXPJQ-UHFFFAOYSA-N 0.000 abstract 1
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 abstract 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005591 Pendimethalin Substances 0.000 abstract 1
- CNILNQMBAHKMFS-UHFFFAOYSA-M Pyrithiobac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(SC=2C(=C(Cl)C=CC=2)C([O-])=O)=N1 CNILNQMBAHKMFS-UHFFFAOYSA-M 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 abstract 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 abstract 1
- 208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 abstract 1
- 229960001701 chloroform Drugs 0.000 abstract 1
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 abstract 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229940113088 dimethylacetamide Drugs 0.000 abstract 1
- SDIXRDNYIMOKSG-UHFFFAOYSA-L disodium methyl arsenate Chemical compound [Na+].[Na+].C[As]([O-])([O-])=O SDIXRDNYIMOKSG-UHFFFAOYSA-L 0.000 abstract 1
- RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 abstract 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 abstract 1
- 229940097068 glyphosate Drugs 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 235000008216 herbs Nutrition 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 abstract 1
- NVGOPFQZYCNLDU-UHFFFAOYSA-N norflurazon Chemical compound O=C1C(Cl)=C(NC)C=NN1C1=CC=CC(C(F)(F)F)=C1 NVGOPFQZYCNLDU-UHFFFAOYSA-N 0.000 abstract 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 abstract 1
- SBUQZKJEOOQSBV-UHFFFAOYSA-N pholedrine Chemical compound CNC(C)CC1=CC=C(O)C=C1 SBUQZKJEOOQSBV-UHFFFAOYSA-N 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Sales de piridilsulfonilureas herbicidamente activas, procesos para su preparación, composiciones que comprenden estos compuestos, y uso de las mismas para controlar hierbas, en particular, en cultivos de plantas cultivadas, o para inhibir el crecimiento de las plantas. Compuestos de fórmula (I), en donde M es un metal alcalino o un metal alcalinoterreo; n es 1 o 2; r y s, independientemente uno del otro, son 0, 1/2, 1, 1 1/2, 2, 2-1/2 ó 3; L es acetato de etilo, acetonitrilo, sulfóxido de dimetilo, formamida, dimetílica, acetamida dimetílica, N-metil-2-pirrolidina, acetona, butanona, cloruro de metileno, triclorometano, tricloroetano, tetrahidrofurano, dietiléter, 1,2-dimetoxietano, dioxano, metiléter de butilo terciario, clorobenceno, tolueno o xileno, con la condición de r sea diferente de 1-1/2 si L es dioxano y s es 0. Los compuestos de la fórmula (I) también se pueden utilizar en combinación con un co-herbicida adecuado, como por ejemplo, ametrina, atracina, hexazinona, asulam, siurón, 2,4-D, halosulfurón, fluometurón, prometina, metolaclor, alfa-metolaclor, norflurazón, piritiobac-sodio, DSMA, MSMA, trifluralina, pendimetalina, bromoxinil, glifosfato, glufosinato y clomazona.Herbicidally active pyridylsulfonylurea salts, processes for their preparation, compositions comprising these compounds, and use thereof to control herbs, in particular in cultivated plant crops, or to inhibit plant growth. Compounds of formula (I), wherein M is an alkali metal or an alkaline earth metal; n is 1 or 2; r and s, independently of each other, are 0, 1/2, 1, 1 1/2, 2, 2-1 / 2 or 3; L is ethyl acetate, acetonitrile, dimethyl sulfoxide, formamide, dimethyl, dimethyl acetamide, N-methyl-2-pyrrolidine, acetone, butanone, methylene chloride, trichloromethane, trichloroethane, tetrahydrofuran, diethyl ether, 1,2-dimethoxyethane, dioxane , tertiary butyl methyl ether, chlorobenzene, toluene or xylene, with the condition of r being different from 1-1 / 2 if L is dioxane and s is 0. The compounds of formula (I) can also be used in combination with a co -suitable herbicide, such as, for example, amethrin, atrazine, hexazinone, asulam, siuron, 2,4-D, halosulfuron, fluometuron, prometin, metolachlor, alpha-metolachlor, norflurazon, pyrithiobac-sodium, DSMA, MSMA, trifluralin, pendimethalin, bromoxynil, glyphosate, glufosinate and clomazone.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH36999 | 1999-03-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UY26044A1 true UY26044A1 (en) | 2000-09-29 |
Family
ID=4185466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UY26044A UY26044A1 (en) | 1999-03-01 | 2000-02-29 | HERBICIDALLY ACTIVE PIRIDILSULFONILUREA SALTS |
Country Status (4)
| Country | Link |
|---|---|
| AU (1) | AU2915700A (en) |
| PE (1) | PE20010035A1 (en) |
| UY (1) | UY26044A1 (en) |
| WO (1) | WO2000052006A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MXPA02007684A (en) * | 2000-02-10 | 2002-12-13 | Syngenta Participations Ag | Novel use of herbicides. |
| WO2003103397A1 (en) * | 2002-06-05 | 2003-12-18 | Syngenta Participations Ag | Herbicidal composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997041112A1 (en) * | 1996-04-25 | 1997-11-06 | Novartis Ag | Sulfonylurea salts as herbicides |
-
2000
- 2000-02-28 AU AU29157/00A patent/AU2915700A/en not_active Abandoned
- 2000-02-28 WO PCT/EP2000/001627 patent/WO2000052006A1/en not_active Ceased
- 2000-02-28 PE PE2000000159A patent/PE20010035A1/en not_active Application Discontinuation
- 2000-02-29 UY UY26044A patent/UY26044A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2915700A (en) | 2000-09-21 |
| PE20010035A1 (en) | 2001-02-15 |
| WO2000052006A1 (en) | 2000-09-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 109 | Application deemed to be withdrawn |
Effective date: 20100319 |