ES329015A2 - Improvements introduced in the preparation of physiologically active compositions. (Machine-translation by Google Translate, not legally binding) - Google Patents
Improvements introduced in the preparation of physiologically active compositions. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES329015A2 ES329015A2 ES0329015A ES329015A ES329015A2 ES 329015 A2 ES329015 A2 ES 329015A2 ES 0329015 A ES0329015 A ES 0329015A ES 329015 A ES329015 A ES 329015A ES 329015 A2 ES329015 A2 ES 329015A2
- Authority
- ES
- Spain
- Prior art keywords
- trifluoromethylbenzimidazole
- nitro
- bromo
- improvements introduced
- translation
- 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
- 239000000203 mixture Substances 0.000 title abstract 3
- 230000027455 binding Effects 0.000 title abstract 2
- 238000009739 binding Methods 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 238000013519 translation Methods 0.000 title abstract 2
- GYDGKROMMMZLQI-UHFFFAOYSA-N 4,6,7-tribromo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Br)C(Br)=C2NC(C(F)(F)F)=NC2=C1Br GYDGKROMMMZLQI-UHFFFAOYSA-N 0.000 abstract 2
- CKEKFQLHCAZGSP-UHFFFAOYSA-N 2-(trifluoromethyl)-3h-benzimidazol-5-amine Chemical compound NC1=CC=C2N=C(C(F)(F)F)NC2=C1 CKEKFQLHCAZGSP-UHFFFAOYSA-N 0.000 abstract 1
- PMISAFNVEGVLSS-UHFFFAOYSA-N 2-(trifluoromethyl)-3h-benzimidazole-5-carbonitrile Chemical compound C1=C(C#N)C=C2NC(C(F)(F)F)=NC2=C1 PMISAFNVEGVLSS-UHFFFAOYSA-N 0.000 abstract 1
- TZMZZAAWGRCWAY-UHFFFAOYSA-N 4,5-dichloro-6-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound ClC1=C(Cl)C([N+](=O)[O-])=CC2=C1N=C(C(F)(F)F)N2 TZMZZAAWGRCWAY-UHFFFAOYSA-N 0.000 abstract 1
- IPVBKOUKUCKNIK-UHFFFAOYSA-N 4,6-dibromo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Br)C=C2NC(C(F)(F)F)=NC2=C1Br IPVBKOUKUCKNIK-UHFFFAOYSA-N 0.000 abstract 1
- ABRYUUSJZZOGOI-UHFFFAOYSA-N 4,6-dichloro-5-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=C(Cl)C=C2NC(C(F)(F)F)=NC2=C1Cl ABRYUUSJZZOGOI-UHFFFAOYSA-N 0.000 abstract 1
- ABJSFSLMGRVNBG-UHFFFAOYSA-N 4,6-dinitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C2N=C(C(F)(F)F)NC2=C1 ABJSFSLMGRVNBG-UHFFFAOYSA-N 0.000 abstract 1
- MWSWJWXZVTVPEQ-UHFFFAOYSA-N 4-bromo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=CC=C2NC(C(F)(F)F)=NC2=C1Br MWSWJWXZVTVPEQ-UHFFFAOYSA-N 0.000 abstract 1
- LUKWKKYXNIHSRJ-UHFFFAOYSA-N 4-bromo-6-chloro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Cl)C=C2NC(C(F)(F)F)=NC2=C1Br LUKWKKYXNIHSRJ-UHFFFAOYSA-N 0.000 abstract 1
- RJHWHAVCPNBCTM-UHFFFAOYSA-N 4-bromo-6-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC(Br)=C2N=C(C(F)(F)F)NC2=C1 RJHWHAVCPNBCTM-UHFFFAOYSA-N 0.000 abstract 1
- XHHVZQKTSKYLQH-UHFFFAOYSA-N 4-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC=CC2=C1N=C(C(F)(F)F)N2 XHHVZQKTSKYLQH-UHFFFAOYSA-N 0.000 abstract 1
- JLNGJAVPDRIMBL-UHFFFAOYSA-N 5,6-dibromo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound BrC1=C(Br)C=C2NC(C(F)(F)F)=NC2=C1 JLNGJAVPDRIMBL-UHFFFAOYSA-N 0.000 abstract 1
- DCCVVWRWIMIAHK-UHFFFAOYSA-N 5,6-dichloro-4-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=CC2=C1N=C(C(F)(F)F)N2 DCCVVWRWIMIAHK-UHFFFAOYSA-N 0.000 abstract 1
- YFYACJUPYYEJMJ-UHFFFAOYSA-N 5-bromo-4-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=C(Br)C=CC2=C1N=C(C(F)(F)F)N2 YFYACJUPYYEJMJ-UHFFFAOYSA-N 0.000 abstract 1
- RGHCRDDIYJEAFI-UHFFFAOYSA-N 5-chloro-4-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=C(Cl)C=CC2=C1N=C(C(F)(F)F)N2 RGHCRDDIYJEAFI-UHFFFAOYSA-N 0.000 abstract 1
- FKSDCMMCSWXZLS-UHFFFAOYSA-N 6-bromo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Br)C=C2NC(C(F)(F)F)=NC2=C1 FKSDCMMCSWXZLS-UHFFFAOYSA-N 0.000 abstract 1
- GQUMVBCXDLOULU-UHFFFAOYSA-N 6-bromo-4-chloro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Br)C=C2NC(C(F)(F)F)=NC2=C1Cl GQUMVBCXDLOULU-UHFFFAOYSA-N 0.000 abstract 1
- USUPLSWSXSTERT-UHFFFAOYSA-N 6-bromo-4-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC(Br)=CC2=C1N=C(C(F)(F)F)N2 USUPLSWSXSTERT-UHFFFAOYSA-N 0.000 abstract 1
- KNWBYYSQLWZITM-UHFFFAOYSA-N 6-chloro-5-nitro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(Cl)C([N+](=O)[O-])=CC2=C1NC(C(F)(F)F)=N2 KNWBYYSQLWZITM-UHFFFAOYSA-N 0.000 abstract 1
- ZZRMDPMUZKDLTO-UHFFFAOYSA-N 6-fluoro-2-(trifluoromethyl)-1h-benzimidazole Chemical compound FC1=CC=C2N=C(C(F)(F)F)NC2=C1 ZZRMDPMUZKDLTO-UHFFFAOYSA-N 0.000 abstract 1
- VWPQFAPZLPFZDE-UHFFFAOYSA-N 6-iodo-2-(trifluoromethyl)-1h-benzimidazole Chemical compound C1=C(I)C=C2NC(C(F)(F)F)=NC2=C1 VWPQFAPZLPFZDE-UHFFFAOYSA-N 0.000 abstract 1
- GPYQJBAVCKSQTJ-UHFFFAOYSA-N 6-methoxy-2-(trifluoromethyl)-1h-benzimidazole Chemical compound COC1=CC=C2N=C(C(F)(F)F)NC2=C1 GPYQJBAVCKSQTJ-UHFFFAOYSA-N 0.000 abstract 1
- OLLDPPSRICPSTA-UHFFFAOYSA-N 6-methyl-2-(trifluoromethyl)-1h-benzimidazole Chemical compound CC1=CC=C2N=C(C(F)(F)F)NC2=C1 OLLDPPSRICPSTA-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000001556 benzimidazoles Chemical class 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/10—Radicals substituted by halogen atoms or nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Improvements introduced in the object of the main patent Nº. 308,860, issued October 29, 1965 by: "Improvements introduced in the preparation of physiologically active compositions", according to which a herbicidal composition contains as an active ingredient at least one substituted benzimidazole selected from: 4-nitro-5-bromo -2-trifluoromethylbenzimidazole, 5-cyano-2-trifluoromethylbenzimidazole, 5-chloro-6-nitro-2-trifluoromethylbenzimidazole, 5-methyl-2-trifluoromethylbenzimidazole, 5-tert.butyl-2-trifluoromethylbenzimidazole, 5-methoxy-2-trifluoromethylbenzimidazole , 5-bromo-2-trifluoromethylbenzimidazole, 5-iodo-2-trifluoromethylbenzimidazole, 5-fluoro-2-trifluoromethylbenzimidazole, 5-amino-2-trifluoromethylbenzimidazole, 4-nitro-2-trifluoromethyl benzimidazole, 4-bromo-2-trifluoromethylbenzimidazole, 4,6-dibromo-2-trifluoromethylbenzimidazole, 5,6-dibromo-2-trifluoromethylbenzimidazole, 4,6,7-tribromo-2-trifluoromethylbenzimidazole, 4-bromo-6-nitro-2-trifluoromethylbenzimidazole, 4-nitro-6 bromo-2-trifluoromethylbenzimidazole, 4-chloro-6-bromo-2-trifluoromethyl benzimidazole, 4-bromo-6-chloro-2-trifluoromethylbenzimidazole, 4,6-dinitro-2-trifluoromethylbenzimidazole, 4-nitro-5-chloro-2-trifluoromethylbenzimidazole, 4-nitro-5,6-dichloro-2-trifluoromethylbenzimidazole, 4,5-dichloro-6-nitro-2-trifluoromethylbenzimidazole, 4,6-dichloro-5-nitro-2-trifluoromethylbenzimidazole and 4,5,7-tribromo-2-trifluoromethylbenzimidazole or their salts. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2958565A GB1147183A (en) | 1965-07-13 | 1965-07-13 | Substituted 2-trifluoromethyl benzimidazoles and their use as herbicides |
| GB3288565 | 1965-07-31 | ||
| GB4498765 | 1965-10-23 | ||
| GB4659465 | 1965-11-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES329015A2 true ES329015A2 (en) | 1967-09-01 |
Family
ID=27448769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0329015A Expired ES329015A2 (en) | 1965-07-13 | 1966-07-12 | Improvements introduced in the preparation of physiologically active compositions. (Machine-translation by Google Translate, not legally binding) |
Country Status (9)
| Country | Link |
|---|---|
| AT (1) | AT279264B (en) |
| BE (1) | BE683812A (en) |
| BR (1) | BR6680830D0 (en) |
| DE (1) | DE1670716A1 (en) |
| ES (1) | ES329015A2 (en) |
| GB (1) | GB1147183A (en) |
| IL (1) | IL26043A (en) |
| NL (1) | NL6609821A (en) |
| NO (1) | NO115276B (en) |
-
1965
- 1965-07-13 GB GB2958565A patent/GB1147183A/en not_active Expired
-
1966
- 1966-06-27 IL IL2604366A patent/IL26043A/en unknown
- 1966-06-30 BR BR18083066A patent/BR6680830D0/en unknown
- 1966-07-05 NO NO16379066A patent/NO115276B/no unknown
- 1966-07-07 BE BE683812D patent/BE683812A/xx unknown
- 1966-07-08 DE DE19661670716 patent/DE1670716A1/en active Pending
- 1966-07-11 AT AT663266A patent/AT279264B/en not_active IP Right Cessation
- 1966-07-12 ES ES0329015A patent/ES329015A2/en not_active Expired
- 1966-07-13 NL NL6609821A patent/NL6609821A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR6680830D0 (en) | 1973-12-04 |
| DE1670716A1 (en) | 1970-12-03 |
| IL26043A (en) | 1970-05-21 |
| NL6609821A (en) | 1967-01-16 |
| BE683812A (en) | 1967-01-09 |
| NO115276B (en) | 1968-09-09 |
| AT279264B (en) | 1970-02-25 |
| GB1147183A (en) | 1969-04-02 |
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