CS220326B2 - Preparation with herbicide,fungicide,growth regulating and defoliating effects - Google Patents
Preparation with herbicide,fungicide,growth regulating and defoliating effects Download PDFInfo
- Publication number
- CS220326B2 CS220326B2 CS802065A CS206580A CS220326B2 CS 220326 B2 CS220326 B2 CS 220326B2 CS 802065 A CS802065 A CS 802065A CS 206580 A CS206580 A CS 206580A CS 220326 B2 CS220326 B2 CS 220326B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- carboxylic acid
- thiadiazole
- methyl
- compounds
- amide
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 8
- 230000000694 effects Effects 0.000 title abstract description 18
- 230000000855 fungicidal effect Effects 0.000 title abstract description 8
- 230000012010 growth Effects 0.000 title abstract description 5
- 230000002363 herbicidal effect Effects 0.000 title abstract description 5
- 230000001105 regulatory effect Effects 0.000 title abstract description 4
- 239000004009 herbicide Substances 0.000 title description 4
- 239000000417 fungicide Substances 0.000 title 1
- -1 cinnamoyl Chemical group 0.000 claims abstract description 56
- 150000001875 compounds Chemical class 0.000 claims abstract description 42
- SZGOQYAJFJBSQD-UHFFFAOYSA-N thiadiazole-5-carboxamide Chemical class NC(=O)C1=CN=NS1 SZGOQYAJFJBSQD-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims abstract description 3
- 125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 claims abstract description 3
- 125000006639 cyclohexyl carbonyl group Chemical group 0.000 claims abstract description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 3
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims abstract description 3
- 125000006331 halo benzoyl group Chemical group 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 2
- 125000006277 halobenzyl group Chemical group 0.000 claims abstract 2
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- CPPCRKJNHYHEQT-UHFFFAOYSA-N n-(cyclohexylmethyl)-4-methylthiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NCC2CCCCC2)=C1C CPPCRKJNHYHEQT-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims description 2
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- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000007244 Zea mays Nutrition 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 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
- 230000008901 benefit Effects 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
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- DJIBHHGQPSAZCY-UHFFFAOYSA-N butoxy-bis(butylsulfanyl)-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCOP(=S)(SCCCC)SCCCC DJIBHHGQPSAZCY-UHFFFAOYSA-N 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000000875 corresponding effect Effects 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229940030980 inova Drugs 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal 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
- PXAQGXWYSIAROF-UHFFFAOYSA-N n,4-dimethylthiadiazole-5-carboxamide Chemical compound CNC(=O)C=1SN=NC=1C PXAQGXWYSIAROF-UHFFFAOYSA-N 0.000 description 1
- JUYMCNMKMHCPMB-UHFFFAOYSA-N n-(cyclohexylmethyl)pentanamide Chemical compound CCCCC(=O)NCC1CCCCC1 JUYMCNMKMHCPMB-UHFFFAOYSA-N 0.000 description 1
- ZOUCHBXJUPPSRN-UHFFFAOYSA-N n-[(2-fluorophenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC=CC=C1F ZOUCHBXJUPPSRN-UHFFFAOYSA-N 0.000 description 1
- WKBSEJMYQYVFJQ-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC=C(Cl)C=C1 WKBSEJMYQYVFJQ-UHFFFAOYSA-N 0.000 description 1
- IHNHPSHMZGCDCL-UHFFFAOYSA-N n-[(4-fluorophenyl)methyl]acetamide Chemical compound CC(=O)NCC1=CC=C(F)C=C1 IHNHPSHMZGCDCL-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
- 150000002825 nitriles Chemical class 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 210000002741 palatine tonsil Anatomy 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 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
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GDPRTNRLCIICFQ-UHFFFAOYSA-N thiadiazole-5-carbonyl chloride Chemical class ClC(=O)C1=CN=NS1 GDPRTNRLCIICFQ-UHFFFAOYSA-N 0.000 description 1
- BXCZJWHJYRELHY-UHFFFAOYSA-N thiadiazole-5-carboxylic acid Chemical class OC(=O)C1=CN=NS1 BXCZJWHJYRELHY-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
Classifications
-
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/06—1,2,3-Thiadiazoles; Hydrogenated 1,2,3-thiadiazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792913977 DE2913977A1 (de) | 1979-04-05 | 1979-04-05 | 1,2,3-thiadiazol-5-carbonsaeureamid- derivate, verfahren zur herstellung dieser verbindungen sowie diese enthaltende mittel mit herbizider, wuchsregulatorischer und entblaetternder sowie fungizider wirkung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS220326B2 true CS220326B2 (en) | 1983-03-25 |
Family
ID=6067688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS802065A CS220326B2 (en) | 1979-04-05 | 1980-03-25 | Preparation with herbicide,fungicide,growth regulating and defoliating effects |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US4314839A (en:Method) |
| JP (1) | JPS55133368A (en:Method) |
| AR (1) | AR223705A1 (en:Method) |
| AT (1) | AT367603B (en:Method) |
| AU (1) | AU535236B2 (en:Method) |
| BE (1) | BE882628A (en:Method) |
| BG (3) | BG32418A3 (en:Method) |
| BR (1) | BR8001999A (en:Method) |
| CA (1) | CA1142945A (en:Method) |
| CH (1) | CH646161A5 (en:Method) |
| CS (1) | CS220326B2 (en:Method) |
| DD (1) | DD149994A5 (en:Method) |
| DE (1) | DE2913977A1 (en:Method) |
| DK (1) | DK146380A (en:Method) |
| ES (1) | ES8200671A1 (en:Method) |
| FR (1) | FR2453165A1 (en:Method) |
| GB (1) | GB2047695B (en:Method) |
| GR (1) | GR66675B (en:Method) |
| HU (1) | HU185216B (en:Method) |
| IE (1) | IE49980B1 (en:Method) |
| IL (1) | IL59737A (en:Method) |
| IT (1) | IT1148809B (en:Method) |
| LU (1) | LU82326A1 (en:Method) |
| NL (1) | NL8001477A (en:Method) |
| PL (1) | PL121775B1 (en:Method) |
| RO (1) | RO79385A (en:Method) |
| SU (1) | SU965355A3 (en:Method) |
| ZA (1) | ZA802033B (en:Method) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3030736A1 (de) * | 1980-08-14 | 1982-03-25 | Basf Ag, 6700 Ludwigshafen | N-disubstituierte anilinderivate, ihre herstellung, ihre verwendung als mikrobizide und mittel dafuer |
| MY113237A (en) * | 1995-03-31 | 2001-12-31 | Nihon Nohyaku Co Ltd | An agricultural and horticultural disease controller and a method for controlling the diseases |
| US6166054A (en) | 1995-03-31 | 2000-12-26 | Nihon Nohyaku Co., Ltd. | Agricultural and horticultural disease controller and a method for controlling the diseases |
| USD421315S (en) | 1995-10-12 | 2000-02-29 | John Manufacturing Limited | Senior signal lantern |
| CA2267471C (en) * | 1996-09-30 | 2004-05-25 | Nihon Nohyaku Co., Ltd. | Bisthiadiazole derivatives and salts thereof, disease controlling agents for agricultural and horticultural use, and method for the use thereof |
| DE69907331T2 (de) * | 1998-07-30 | 2003-10-23 | Nihon Nohyaku Co., Ltd. | Fungizide Zusammensetzung enthaltend ein 1,2,3-Thiadiazolderivat sowie deren Verwendung |
| KR100700964B1 (ko) * | 2000-03-15 | 2007-03-28 | 니혼노야쿠가부시키가이샤 | 살충살균제 조성물 및 그의 사용방법 |
| AR056882A1 (es) * | 2006-02-01 | 2007-10-31 | Bayer Cropscience Sa | Derivados del fungicida n- cicloalquil- bencil- amida |
| CN101250168B (zh) * | 2008-03-28 | 2011-12-14 | 南开大学 | 噻二唑亚胺衍生物及其合成方法和用途 |
| GB201818350D0 (en) * | 2018-11-12 | 2018-12-26 | Syngenta Participations Ag | Herbicidal compounds |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2728523C2 (de) * | 1977-06-23 | 1986-02-27 | Schering AG, 1000 Berlin und 4709 Bergkamen | 4-Methyl-1,2,3-thiadiazol-5-carbonsäure-(cyclohexylmethyl)-amid, Mittel mit herbizider und wachstumsregulatorischer Wirkung enthaltend diese Verbindung sowie Verfahren zu seiner Herstellung |
| US4163784A (en) * | 1978-03-09 | 1979-08-07 | Pfizer Inc. | Heterocyclylcarbonyl derivatives of urea, agents for dissolution of gallstones |
-
1979
- 1979-04-05 DE DE19792913977 patent/DE2913977A1/de not_active Withdrawn
-
1980
- 1980-03-12 NL NL8001477A patent/NL8001477A/nl not_active Application Discontinuation
- 1980-03-18 US US06/131,354 patent/US4314839A/en not_active Expired - Lifetime
- 1980-03-25 CS CS802065A patent/CS220326B2/cs unknown
- 1980-03-28 ES ES490069A patent/ES8200671A1/es not_active Expired
- 1980-03-31 GB GB8010811A patent/GB2047695B/en not_active Expired
- 1980-03-31 IL IL59737A patent/IL59737A/xx unknown
- 1980-04-01 SU SU802903448A patent/SU965355A3/ru active
- 1980-04-01 BR BR8001999A patent/BR8001999A/pt unknown
- 1980-04-01 IT IT21094/80A patent/IT1148809B/it active
- 1980-04-01 CA CA000348941A patent/CA1142945A/en not_active Expired
- 1980-04-01 CH CH255780A patent/CH646161A5/de not_active IP Right Cessation
- 1980-04-02 AT AT0180780A patent/AT367603B/de not_active IP Right Cessation
- 1980-04-02 AR AR280536A patent/AR223705A1/es active
- 1980-04-02 BG BG047213A patent/BG32418A3/xx unknown
- 1980-04-02 GR GR61617A patent/GR66675B/el unknown
- 1980-04-02 BG BG048538A patent/BG32414A3/xx unknown
- 1980-04-02 BG BG049349A patent/BG32415A3/xx unknown
- 1980-04-02 DK DK146380A patent/DK146380A/da not_active IP Right Cessation
- 1980-04-03 HU HU80819A patent/HU185216B/hu unknown
- 1980-04-03 IE IE680/80A patent/IE49980B1/en unknown
- 1980-04-03 BE BE0/200113A patent/BE882628A/fr not_active IP Right Cessation
- 1980-04-03 AU AU57152/80A patent/AU535236B2/en not_active Ceased
- 1980-04-03 LU LU82326A patent/LU82326A1/de unknown
- 1980-04-03 ZA ZA00802033A patent/ZA802033B/xx unknown
- 1980-04-03 PL PL1980223230A patent/PL121775B1/pl unknown
- 1980-04-03 DD DD80220211A patent/DD149994A5/de unknown
- 1980-04-04 JP JP4453480A patent/JPS55133368A/ja active Pending
- 1980-04-04 FR FR8007671A patent/FR2453165A1/fr active Granted
- 1980-04-07 RO RO80100723A patent/RO79385A/ro unknown
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