SU862811A3 - Гербицидна композици - Google Patents
Гербицидна композици Download PDFInfo
- Publication number
- SU862811A3 SU862811A3 SU711726247A SU1726247A SU862811A3 SU 862811 A3 SU862811 A3 SU 862811A3 SU 711726247 A SU711726247 A SU 711726247A SU 1726247 A SU1726247 A SU 1726247A SU 862811 A3 SU862811 A3 SU 862811A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- benzoyl
- formula
- propionitrile
- prepared
- group
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 12
- 239000000203 mixture Substances 0.000 title claims abstract description 11
- 239000004009 herbicide Substances 0.000 title abstract description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 239000013543 active substance Substances 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 239000003995 emulsifying agent Substances 0.000 claims 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 3
- 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 description 2
- 229910052717 sulfur Inorganic materials 0.000 abstract description 2
- 239000004094 surface-active agent Substances 0.000 abstract description 2
- 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
- 150000003839 salts Chemical class 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
- 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
- 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
- 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
- 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
- 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
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000001424 substituent group Chemical group 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
- 241000196324 Embryophyta Species 0.000 description 5
- 150000001448 anilines Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 241000209761 Avena Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 241000894007 species Species 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 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 |
|---|---|
| SU862811A3 true SU862811A3 (ru) | 1981-09-07 |
Family
ID=10484289
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU711726247A SU862811A3 (ru) | 1970-12-16 | 1971-12-14 | Гербицидна композици |
Country Status (6)
| Country | Link |
|---|---|
| AU (1) | AU465502B2 (cg-RX-API-DMAC10.html) |
| CA (1) | CA970388A (cg-RX-API-DMAC10.html) |
| FR (1) | FR2118588A5 (cg-RX-API-DMAC10.html) |
| GB (1) | GB1355349A (cg-RX-API-DMAC10.html) |
| HU (1) | HU164833B (cg-RX-API-DMAC10.html) |
| SU (1) | SU862811A3 (cg-RX-API-DMAC10.html) |
-
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 |
| GB1355349A (en) | 1974-06-05 |
| FR2118588A5 (cg-RX-API-DMAC10.html) | 1972-07-28 |
| AU465502B2 (en) | 1975-10-02 |
| HU164833B (cg-RX-API-DMAC10.html) | 1974-04-11 |
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