NO792575L - 1,2,3-triazolcarboxylsyreamider, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disse - Google Patents
1,2,3-triazolcarboxylsyreamider, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disseInfo
- Publication number
- NO792575L NO792575L NO792575A NO792575A NO792575L NO 792575 L NO792575 L NO 792575L NO 792575 A NO792575 A NO 792575A NO 792575 A NO792575 A NO 792575A NO 792575 L NO792575 L NO 792575L
- Authority
- NO
- Norway
- Prior art keywords
- triazole
- carboxylic acid
- amide
- ethyl
- propylsulfonyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 13
- 239000003139 biocide Substances 0.000 title claims description 6
- 238000002360 preparation method Methods 0.000 title description 14
- GTODOEDLCNTSLG-UHFFFAOYSA-N 2h-triazole-4-carboxylic acid Chemical compound OC(=O)C1=CNN=N1 GTODOEDLCNTSLG-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 46
- -1 morpholino- Chemical class 0.000 claims description 33
- MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical compound [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 claims description 28
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 claims description 27
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 17
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 12
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- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 125000000304 alkynyl group Chemical group 0.000 claims description 10
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 9
- OSKSVLBJJXQUPI-UHFFFAOYSA-N 2h-triazole-4-carboxamide Chemical class NC(=O)C1=CNN=N1 OSKSVLBJJXQUPI-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 claims description 8
- 230000002363 herbicidal effect Effects 0.000 claims description 8
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- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- 239000000417 fungicide Substances 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 239000012948 isocyanate Substances 0.000 claims description 5
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- 238000004519 manufacturing process Methods 0.000 claims description 5
- 150000000177 1,2,3-triazoles Chemical class 0.000 claims description 4
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- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
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- 239000002917 insecticide Substances 0.000 claims description 4
- 230000001069 nematicidal effect Effects 0.000 claims description 4
- OJKZEZMAPKWHTG-UHFFFAOYSA-N bis(2h-triazol-4-yl)methanone Chemical class C=1NN=NC=1C(=O)C1=CNN=N1 OJKZEZMAPKWHTG-UHFFFAOYSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 230000000749 insecticidal effect Effects 0.000 claims description 3
- 150000002736 metal compounds Chemical class 0.000 claims description 3
- 125000005394 methallyl group Chemical group 0.000 claims description 3
- 150000007530 organic bases Chemical class 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 150000002641 lithium Chemical group 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
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- 239000001301 oxygen Substances 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 claims 14
- MSZJEPVVQWJCIF-UHFFFAOYSA-N butylazanide Chemical compound CCCC[NH-] MSZJEPVVQWJCIF-UHFFFAOYSA-N 0.000 claims 5
- PBGGNZZGJIKBMJ-UHFFFAOYSA-N di(propan-2-yl)azanide Chemical compound CC(C)[N-]C(C)C PBGGNZZGJIKBMJ-UHFFFAOYSA-N 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- JLLYLQLDYORLBB-UHFFFAOYSA-N 5-bromo-n-methylthiophene-2-sulfonamide Chemical compound CNS(=O)(=O)C1=CC=C(Br)S1 JLLYLQLDYORLBB-UHFFFAOYSA-N 0.000 claims 4
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims 4
- ABBZJHFBQXYTLU-UHFFFAOYSA-N but-3-enamide Chemical compound NC(=O)CC=C ABBZJHFBQXYTLU-UHFFFAOYSA-N 0.000 claims 3
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 claims 3
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims 2
- WCYBYZBPWZTMDW-UHFFFAOYSA-N dibutylazanide Chemical compound CCCC[N-]CCCC WCYBYZBPWZTMDW-UHFFFAOYSA-N 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- NJBCRXCAPCODGX-UHFFFAOYSA-N 2-methyl-n-(2-methylpropyl)propan-1-amine Chemical compound CC(C)CNCC(C)C NJBCRXCAPCODGX-UHFFFAOYSA-N 0.000 claims 1
- JFVZQTWACVPVHC-UHFFFAOYSA-N 4-propan-2-ylsulfanyl-2h-triazole Chemical compound CC(C)SC=1C=NNN=1 JFVZQTWACVPVHC-UHFFFAOYSA-N 0.000 claims 1
- TXFLGZOGNOOEFZ-UHFFFAOYSA-N bis(2-chloroethyl)amine Chemical compound ClCCNCCCl TXFLGZOGNOOEFZ-UHFFFAOYSA-N 0.000 claims 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 claims 1
- HVAAHUDGWQAAOJ-UHFFFAOYSA-N n-benzylethanamine Chemical compound CCNCC1=CC=CC=C1 HVAAHUDGWQAAOJ-UHFFFAOYSA-N 0.000 claims 1
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- XUWVIABDWDTJRZ-UHFFFAOYSA-N propan-2-ylazanide Chemical compound CC(C)[NH-] XUWVIABDWDTJRZ-UHFFFAOYSA-N 0.000 claims 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- UXHMGTYELGTNSJ-UHFFFAOYSA-N triazole-1-carboxamide Chemical class NC(=O)N1C=CN=N1 UXHMGTYELGTNSJ-UHFFFAOYSA-N 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 32
- 239000013543 active substance Substances 0.000 description 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
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- 235000007164 Oryza sativa Nutrition 0.000 description 1
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- 241000124033 Salix Species 0.000 description 1
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- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 230000003851 biochemical process Effects 0.000 description 1
- 150000001715 carbamic acids Chemical class 0.000 description 1
- 230000021235 carbamoylation Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
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- 239000002270 dispersing agent Substances 0.000 description 1
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- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 238000003197 gene knockdown Methods 0.000 description 1
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- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000003977 halocarboxylic acids Chemical class 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004660 morphological change Effects 0.000 description 1
- OWRABTHGOKNUDV-UHFFFAOYSA-N n,n-dipropylcarbamoyl chloride Chemical compound CCCN(C(Cl)=O)CCC OWRABTHGOKNUDV-UHFFFAOYSA-N 0.000 description 1
- KCNUWLJAWRWKMO-UHFFFAOYSA-N n-ethyl-n-propyl-3-propylsulfonyl-1,2,4-triazole-1-carboxamide Chemical compound CCCN(CC)C(=O)N1C=NC(S(=O)(=O)CCC)=N1 KCNUWLJAWRWKMO-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
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- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 230000021749 root development Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
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- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
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- 238000003892 spreading Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
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- 230000002195 synergetic effect Effects 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003560 thiocarbamic acids Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782834879 DE2834879A1 (de) | 1978-08-07 | 1978-08-07 | 1,2,3-triazolcarbonsaeureamide, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO792575L true NO792575L (no) | 1980-02-08 |
Family
ID=6046591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO792575A NO792575L (no) | 1978-08-07 | 1979-08-06 | 1,2,3-triazolcarboxylsyreamider, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disse |
Country Status (38)
| Country | Link |
|---|---|
| US (1) | US4233059A (fr) |
| JP (1) | JPS5524179A (fr) |
| AR (1) | AR222039A1 (fr) |
| AT (1) | AT365892B (fr) |
| AU (1) | AU523909B2 (fr) |
| BE (1) | BE878127A (fr) |
| BR (1) | BR7905011A (fr) |
| CA (1) | CA1129425A (fr) |
| CH (1) | CH640518A5 (fr) |
| CS (1) | CS205149B2 (fr) |
| DD (1) | DD145364A5 (fr) |
| DE (1) | DE2834879A1 (fr) |
| DK (1) | DK301879A (fr) |
| EG (1) | EG14370A (fr) |
| ES (1) | ES483115A1 (fr) |
| FI (1) | FI792423A (fr) |
| FR (1) | FR2433018A1 (fr) |
| GB (1) | GB2028319B (fr) |
| GR (1) | GR72718B (fr) |
| IE (1) | IE48787B1 (fr) |
| IL (1) | IL57927A (fr) |
| IN (1) | IN152609B (fr) |
| IT (1) | IT1122324B (fr) |
| LU (1) | LU81578A1 (fr) |
| MA (1) | MA18557A1 (fr) |
| MX (1) | MX5623E (fr) |
| NL (1) | NL7904611A (fr) |
| NO (1) | NO792575L (fr) |
| NZ (1) | NZ191185A (fr) |
| PH (1) | PH16769A (fr) |
| PL (1) | PL118237B1 (fr) |
| PT (1) | PT69999A (fr) |
| RO (2) | RO81505B (fr) |
| SE (1) | SE7906602L (fr) |
| SU (1) | SU929008A3 (fr) |
| TR (1) | TR20593A (fr) |
| YU (1) | YU149179A (fr) |
| ZA (1) | ZA794084B (fr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4280831A (en) * | 1980-08-04 | 1981-07-28 | Gulf Oil Corporation | Benzylsulfonyl diethylcarbamyl triazole and use as a selective herbicide |
| US4596597A (en) * | 1985-06-21 | 1986-06-24 | Stauffer Chemical Company | Esters of 1,2 and 3-N,N-dialkylcarbamyl-5-substituted-1H-1,2,3-triazole-4-carboxylic acid |
| US4596596A (en) * | 1985-06-21 | 1986-06-24 | Stauffer Chemical Company | 1-,2-,and 3-N,N-dialkylcarbamyl-1-H-1,2,3-triazoles |
| JPH0559017A (ja) * | 1990-10-26 | 1993-03-09 | Ube Ind Ltd | １，２，３−トリアゾール誘導体、その製法及び有害生物防除剤 |
| PL375353A1 (en) * | 2002-08-22 | 2005-11-28 | Syngenta Participations Ag | Chemical compounds |
| NZ593418A (en) * | 2008-12-24 | 2013-10-25 | Bial Portela & Ca Sa | Imidazole compounds for use as enzyme inhibitors |
| CA2830958A1 (fr) * | 2011-04-06 | 2012-10-11 | The Scripps Research Institute | Inhibiteurs des serine hydrolases de type n1- et n2-carbamoyl-1,2,3-triazole et methodes associees |
| CN102775361B (zh) * | 2012-07-27 | 2014-11-12 | 浙江工业大学 | 一种1,2,4-三唑类衍生物、其制备方法及用途 |
| US11085342B2 (en) | 2018-06-20 | 2021-08-10 | Ngk Insulators, Ltd. | Honeycomb filter |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3952001A (en) | 1970-07-01 | 1976-04-20 | The Boots Company Limited | 1-Carbamoyl-1,2,4-triazoles |
-
1978
- 1978-08-07 DE DE19782834879 patent/DE2834879A1/de not_active Withdrawn
-
1979
- 1979-06-12 NL NL7904611A patent/NL7904611A/nl not_active Application Discontinuation
- 1979-06-25 YU YU01491/79A patent/YU149179A/xx unknown
- 1979-07-13 AR AR277299A patent/AR222039A1/es active
- 1979-07-13 IN IN507/DEL/79A patent/IN152609B/en unknown
- 1979-07-18 DK DK301879A patent/DK301879A/da not_active Application Discontinuation
- 1979-07-18 CS CS795021A patent/CS205149B2/cs unknown
- 1979-07-25 IT IT24631/79A patent/IT1122324B/it active
- 1979-07-30 CA CA332,838A patent/CA1129425A/fr not_active Expired
- 1979-07-30 PT PT69999A patent/PT69999A/pt unknown
- 1979-07-30 GB GB7926412A patent/GB2028319B/en not_active Expired
- 1979-07-31 IL IL57927A patent/IL57927A/xx unknown
- 1979-08-01 US US06/062,795 patent/US4233059A/en not_active Expired - Lifetime
- 1979-08-01 NZ NZ191185A patent/NZ191185A/xx unknown
- 1979-08-02 MX MX798297U patent/MX5623E/es unknown
- 1979-08-02 DD DD79214769A patent/DD145364A5/de unknown
- 1979-08-03 ES ES483115A patent/ES483115A1/es not_active Expired
- 1979-08-03 MA MA18755A patent/MA18557A1/fr unknown
- 1979-08-03 FI FI792423A patent/FI792423A/fi not_active Application Discontinuation
- 1979-08-06 FR FR7920083A patent/FR2433018A1/fr active Granted
- 1979-08-06 PH PH22864A patent/PH16769A/en unknown
- 1979-08-06 EG EG476/79A patent/EG14370A/xx active
- 1979-08-06 RO RO103432A patent/RO81505B/ro unknown
- 1979-08-06 SE SE7906602A patent/SE7906602L/xx unknown
- 1979-08-06 PL PL1979217595A patent/PL118237B1/pl unknown
- 1979-08-06 LU LU81578A patent/LU81578A1/de unknown
- 1979-08-06 BR BR7905011A patent/BR7905011A/pt unknown
- 1979-08-06 CH CH721279A patent/CH640518A5/de not_active IP Right Cessation
- 1979-08-06 SU SU792797788A patent/SU929008A3/ru active
- 1979-08-06 NO NO792575A patent/NO792575L/no unknown
- 1979-08-06 TR TR20593A patent/TR20593A/xx unknown
- 1979-08-06 RO RO7998383A patent/RO77561A/fr unknown
- 1979-08-06 GR GR59781A patent/GR72718B/el unknown
- 1979-08-06 AT AT0536579A patent/AT365892B/de not_active IP Right Cessation
- 1979-08-06 AU AU49594/79A patent/AU523909B2/en not_active Ceased
- 1979-08-07 JP JP9993379A patent/JPS5524179A/ja active Pending
- 1979-08-07 ZA ZA00794084A patent/ZA794084B/xx unknown
- 1979-08-07 BE BE0/196637A patent/BE878127A/fr not_active IP Right Cessation
- 1979-08-08 IE IE1488/79A patent/IE48787B1/en unknown
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