SU482930A3 - Фунгицид - Google Patents
ФунгицидInfo
- Publication number
- SU482930A3 SU482930A3 SU1382947A SU1382947A SU482930A3 SU 482930 A3 SU482930 A3 SU 482930A3 SU 1382947 A SU1382947 A SU 1382947A SU 1382947 A SU1382947 A SU 1382947A SU 482930 A3 SU482930 A3 SU 482930A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- alkyl
- nutrient solution
- group
- chlorine
- carbon atoms
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title description 3
- 230000000855 fungicidal effect Effects 0.000 title description 2
- 235000015097 nutrients Nutrition 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 125000001309 chloro group Chemical group Cl* 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 239000013543 active substance Substances 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 2
- 241000228212 Aspergillus Species 0.000 description 2
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 241000427940 Fusarium solani Species 0.000 description 2
- 239000008272 agar Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- -1 Ci- alkyl Chemical group 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 238000009736 wetting Methods 0.000 description 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
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19681812100 DE1812100C3 (de) | 1968-12-02 | Substituierte i-Carbamoyl-2-carbalkoxyamlnobenzlmldazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU482930A3 true SU482930A3 (ru) | 1975-08-30 |
Family
ID=5714917
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1382947A SU482930A3 (ru) | 1968-12-02 | 1969-11-25 | Фунгицид |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US3660421A (https=) |
| AT (1) | AT297402B (https=) |
| BE (1) | BE742452A (https=) |
| CH (1) | CH536596A (https=) |
| DK (1) | DK125506B (https=) |
| ES (1) | ES374142A1 (https=) |
| FR (1) | FR2027563A1 (https=) |
| GB (1) | GB1287157A (https=) |
| IL (1) | IL33428A (https=) |
| MY (1) | MY7300211A (https=) |
| NL (1) | NL6917807A (https=) |
| OA (1) | OA03183A (https=) |
| SE (1) | SE371198B (https=) |
| SU (1) | SU482930A3 (https=) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3993769A (en) * | 1972-12-29 | 1976-11-23 | Syntex (U.S.A.) Inc. | 1,5(6)-Disubstituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
| CA1032171A (en) * | 1972-12-29 | 1978-05-30 | Colin C. Beard | 5(6)-benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
| US4078070A (en) * | 1973-01-16 | 1978-03-07 | Hoechst Aktiengesellschaft | Fungicidal dispersions |
| DE2303999A1 (de) * | 1973-01-27 | 1974-08-08 | Hoechst Ag | Substituierte benzimidazole |
| JPS5825674B2 (ja) * | 1973-03-27 | 1983-05-28 | 三共株式会社 | ベンズイミダゾ−ルカルバミンサンエステルルイノ セイゾウホウ |
| JPS5826343B2 (ja) * | 1973-05-31 | 1983-06-02 | 日本曹達株式会社 | ベンズイミダゾ−ルユウドウタイ ノ セイゾウホウ |
| JPS5032175A (https=) * | 1973-07-24 | 1975-03-28 | ||
| DE2347386A1 (de) * | 1973-09-17 | 1975-04-03 | Schering Ag | Benzimidazol-1-carbonsaeureamide |
| US3929823A (en) * | 1973-11-21 | 1975-12-30 | Syntex Inc | 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives having anthelmintic activity |
| FR2324635A1 (fr) * | 1975-09-17 | 1977-04-15 | Univ Syracuse Res Corp | ((alcoxyalkylcarbamoyl-1)benzimidazolyl-2)carbamates d'alkyle, leur preparation et leur emploi comme pesticides |
| US4828542A (en) * | 1986-08-29 | 1989-05-09 | Twin Rivers Engineering | Foam substrate and micropackaged active ingredient particle composite dispensing materials |
| US5098621A (en) * | 1985-01-07 | 1992-03-24 | Twin Rivers Engineering | Method of forming a foam substrate and micropackaged active ingredient particle composite |
-
1969
- 1969-11-25 US US879937A patent/US3660421A/en not_active Expired - Lifetime
- 1969-11-25 IL IL33428A patent/IL33428A/en unknown
- 1969-11-25 SU SU1382947A patent/SU482930A3/ru active
- 1969-11-26 FR FR6940770A patent/FR2027563A1/fr not_active Withdrawn
- 1969-11-26 NL NL6917807A patent/NL6917807A/xx unknown
- 1969-11-28 SE SE6916457A patent/SE371198B/xx unknown
- 1969-11-28 CH CH1779769A patent/CH536596A/de not_active IP Right Cessation
- 1969-12-01 BE BE742452D patent/BE742452A/xx unknown
- 1969-12-01 DK DK635469AA patent/DK125506B/da unknown
- 1969-12-01 OA OA53798A patent/OA03183A/xx unknown
- 1969-12-01 GB GB58505/69A patent/GB1287157A/en not_active Expired
- 1969-12-01 AT AT1121169A patent/AT297402B/de not_active IP Right Cessation
- 1969-12-02 ES ES374142A patent/ES374142A1/es not_active Expired
-
1973
- 1973-12-30 MY MY211/73A patent/MY7300211A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE742452A (https=) | 1970-06-01 |
| DE1812100A1 (de) | 1970-06-11 |
| IL33428A0 (en) | 1970-01-29 |
| IL33428A (en) | 1972-12-29 |
| AT297402B (de) | 1972-03-27 |
| US3660421A (en) | 1972-05-02 |
| SE371198B (https=) | 1974-11-11 |
| GB1287157A (en) | 1972-08-31 |
| FR2027563A1 (https=) | 1970-10-02 |
| NL6917807A (https=) | 1970-06-04 |
| MY7300211A (en) | 1973-12-31 |
| CH536596A (de) | 1973-05-15 |
| ES374142A1 (es) | 1972-03-16 |
| OA03183A (fr) | 1970-12-15 |
| DK125506B (da) | 1973-03-05 |
| DE1812100B2 (de) | 1976-01-02 |
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