GB1355349A - N,n-disubstituted amino -thio- carboximidic esters and salts thereof and their use as herbicides - Google Patents
N,n-disubstituted amino -thio- carboximidic esters and salts thereof and their use as herbicidesInfo
- Publication number
- GB1355349A GB1355349A GB1355349DA GB1355349A GB 1355349 A GB1355349 A GB 1355349A GB 1355349D A GB1355349D A GB 1355349DA GB 1355349 A GB1355349 A GB 1355349A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzoyl
- propionitrile
- formula
- carboximidic
- thio
- 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
- 150000003839 salts Chemical class 0.000 title abstract 3
- 239000004009 herbicide Substances 0.000 title abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 title abstract 2
- 150000002148 esters Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- OBJMWYAZGBFFNS-UHFFFAOYSA-N 2-anilinopropanenitrile Chemical compound N#CC(C)NC1=CC=CC=C1 OBJMWYAZGBFFNS-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract 1
- LQVUUGHQHYFSCN-UHFFFAOYSA-N N-(1-cyanoethyl)-N-(3,4-dichlorophenyl)benzamide Chemical compound C(C1=CC=CC=C1)(=O)N(C1=CC(=C(C=C1)Cl)Cl)C(C#N)C LQVUUGHQHYFSCN-UHFFFAOYSA-N 0.000 abstract 1
- UWFQSPRJQSWMKK-UHFFFAOYSA-N N-(1-cyanoethyl)-N-(4-fluorophenyl)benzamide Chemical compound C(C1=CC=CC=C1)(=O)N(C1=CC=C(C=C1)F)C(C#N)C UWFQSPRJQSWMKK-UHFFFAOYSA-N 0.000 abstract 1
- WPTBTIATDOKXQU-UHFFFAOYSA-N N-(4-chloro-3-fluorophenyl)-N-(1-cyanoethyl)benzamide Chemical compound C(C1=CC=CC=C1)(=O)N(C1=CC(=C(C=C1)Cl)F)C(C#N)C WPTBTIATDOKXQU-UHFFFAOYSA-N 0.000 abstract 1
- MEHVYMNCAQNRTE-UHFFFAOYSA-N N-(4-chlorophenyl)-N-(1-cyanoethyl)benzamide Chemical compound C(C1=CC=CC=C1)(=O)N(C1=CC=C(C=C1)Cl)C(C#N)C MEHVYMNCAQNRTE-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 abstract 1
- 229920001577 copolymer Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5971870 | 1970-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1355349A true GB1355349A (en) | 1974-06-05 |
Family
ID=10484289
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1355349D Expired GB1355349A (en) | 1970-12-16 | 1970-12-16 | N,n-disubstituted amino -thio- carboximidic esters and salts thereof and their use as herbicides |
Country Status (6)
| Country | Link |
|---|---|
| AU (1) | AU465502B2 (enExample) |
| CA (1) | CA970388A (enExample) |
| FR (1) | FR2118588A5 (enExample) |
| GB (1) | GB1355349A (enExample) |
| HU (1) | HU164833B (enExample) |
| SU (1) | SU862811A3 (enExample) |
-
1970
- 1970-12-16 GB GB1355349D patent/GB1355349A/en not_active Expired
-
1971
- 1971-12-14 SU SU711726247A patent/SU862811A3/ru active
- 1971-12-14 CA CA130,133A patent/CA970388A/en not_active Expired
- 1971-12-14 FR FR7144848A patent/FR2118588A5/fr not_active Expired
- 1971-12-14 AU AU36847/71A patent/AU465502B2/en not_active Expired
- 1971-12-14 HU HUSE001599 patent/HU164833B/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU3684771A (en) | 1973-06-21 |
| CA970388A (en) | 1975-07-01 |
| SU862811A3 (ru) | 1981-09-07 |
| FR2118588A5 (enExample) | 1972-07-28 |
| AU465502B2 (en) | 1975-10-02 |
| HU164833B (enExample) | 1974-04-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |