GB1025049A - Carbamic acid esters - Google Patents
Carbamic acid estersInfo
- Publication number
- GB1025049A GB1025049A GB3262/65A GB326265A GB1025049A GB 1025049 A GB1025049 A GB 1025049A GB 3262/65 A GB3262/65 A GB 3262/65A GB 326265 A GB326265 A GB 326265A GB 1025049 A GB1025049 A GB 1025049A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkylmercapto
- alkoxy
- alkenylmercapto
- dialkenylamino
- cycloalkoxy
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 229940112021 centrally acting muscle relaxants carbamic acid ester Drugs 0.000 title 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 title 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 230000003115 biocidal effect Effects 0.000 abstract 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229940100892 mercury compound Drugs 0.000 abstract 1
- 150000002731 mercury compounds Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/12—Radicals substituted by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of formula <FORM:1025049/C2/1> wherein R1 is H, halogen, alkyl, alkenyl, alkoxy, dialkylamino, dialkenylamino, alkylmercapto, alkenylmercapto or nitro, n is 1-5, A is C1- 10 alkylene and R2 is Cl, alkoxy, cycloalkoxy, alkylmercapto or a heterocyclic radical, These compounds are made from the parent phenol by reaction with (a) R2-A-NCO or (b) COCl2 to give the corresponding chloroformate or carbonate, which is then reacted with R2-A-NH2.ALSO:A method of combating fungi comprises treating plants or soil with a compound of formula <FORM:1025049/A5-A6/1> wherein R1 is H1 halogen, alkyl, alkenyl, alkoxy, dialkylamino, dialkenylamino, alkylmercapto, alkenylmercapto or nitro, n is 1-5, A is C1-10 alkylene and R2 is Cl, alkoxy, cycloalkoxy, alkylmercapto or a heterocyclic radical; alone, or in admixture with a solid or liquid diluent or carrier and optionally with the addition of an organic mercury compound and/or an antibiotic. Emulsifiers and dispersing agents may also be used and the fungicidal compositions are utilized in the usual forms such as emulsifiable concentrates, spray powders, pastes, soluble powders, dusts and granulates.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0041833 | 1964-01-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1025049A true GB1025049A (en) | 1966-04-06 |
Family
ID=7098832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3262/65A Expired GB1025049A (en) | 1964-01-25 | 1965-01-25 | Carbamic acid esters |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3376335A (en) |
| BE (1) | BE658752A (en) |
| CH (1) | CH441861A (en) |
| ES (2) | ES308529A1 (en) |
| FR (1) | FR1452615A (en) |
| GB (1) | GB1025049A (en) |
| IL (1) | IL22692A (en) |
| NL (1) | NL6500915A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3865866A (en) * | 1970-01-30 | 1975-02-11 | Sumitomo Chemical Co | Carbamic acid esters |
| US4812590A (en) * | 1987-06-25 | 1989-03-14 | Merck & Co., Inc. | Carbamates of 4-hydroxyanisole as prodrugs for chemotherapy of melanoma |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE632152A (en) * | ||||
| US2945780A (en) * | 1955-03-24 | 1960-07-19 | Fmc Corp | Synergistic insecticidal compositions |
| US3131213A (en) * | 1957-05-21 | 1964-04-28 | Sterling Drug Inc | 2, 6-dimethyl and 2, 6-diethylphenyl n-(aminoalkyl) carbamates and acid addition salts thereof |
| DE1139113B (en) * | 1961-01-17 | 1962-11-08 | Basf Ag | Process for the preparation of N-ª ‰ -haloalkylcarbamic acid esters |
| NL276002A (en) * | 1961-03-21 |
-
1964
- 1964-12-28 CH CH1670264A patent/CH441861A/en unknown
- 1964-12-29 IL IL22692A patent/IL22692A/en unknown
-
1965
- 1965-01-05 US US423596A patent/US3376335A/en not_active Expired - Lifetime
- 1965-01-25 GB GB3262/65A patent/GB1025049A/en not_active Expired
- 1965-01-25 FR FR3219A patent/FR1452615A/en not_active Expired
- 1965-01-25 ES ES0308529A patent/ES308529A1/en not_active Expired
- 1965-01-25 NL NL6500915A patent/NL6500915A/xx unknown
- 1965-01-25 BE BE658752D patent/BE658752A/xx unknown
- 1965-03-23 ES ES0310863A patent/ES310863A1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US3376335A (en) | 1968-04-02 |
| NL6500915A (en) | 1965-07-26 |
| ES310863A1 (en) | 1965-12-16 |
| CH441861A (en) | 1967-08-15 |
| ES308529A1 (en) | 1965-05-01 |
| IL22692A (en) | 1968-07-25 |
| FR1452615A (en) | 1966-04-15 |
| BE658752A (en) | 1965-07-26 |
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