DD141257A5 - Pestizide bzw.pflanzenwachstumsregulierende zusammensetzungen - Google Patents
Pestizide bzw.pflanzenwachstumsregulierende zusammensetzungen Download PDFInfo
- Publication number
- DD141257A5 DD141257A5 DD78208817A DD20881778A DD141257A5 DD 141257 A5 DD141257 A5 DD 141257A5 DD 78208817 A DD78208817 A DD 78208817A DD 20881778 A DD20881778 A DD 20881778A DD 141257 A5 DD141257 A5 DD 141257A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- ethyl
- alkyl
- substituted
- carboxylate
- aryl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 44
- 239000000575 pesticide Substances 0.000 title claims description 14
- -1 nitro, amino, substituted amino Chemical group 0.000 claims abstract description 74
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 52
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 33
- 239000001257 hydrogen Substances 0.000 claims abstract description 29
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 22
- 150000002367 halogens Chemical group 0.000 claims abstract description 22
- 125000003118 aryl group Chemical group 0.000 claims abstract description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 16
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims abstract description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 10
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- 125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 10
- 125000003107 substituted aryl group Chemical group 0.000 claims abstract description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 9
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 7
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- 239000011593 sulfur Chemical group 0.000 claims abstract description 5
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- WABRGVKKLPDKAC-UHFFFAOYSA-N 1,2-oxazol-5-ylurea Chemical compound NC(=O)NC1=CC=NO1 WABRGVKKLPDKAC-UHFFFAOYSA-N 0.000 claims abstract description 3
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- 125000001424 substituent group Chemical group 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 18
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
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- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
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- 150000003956 methylamines Chemical class 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- DWLVWMUCHSLGSU-UHFFFAOYSA-M n,n-dimethylcarbamate Chemical compound CN(C)C([O-])=O DWLVWMUCHSLGSU-UHFFFAOYSA-M 0.000 description 1
- HPTQNIZSFRLFIU-UHFFFAOYSA-N n-(4-chlorophenyl)-2-hydroxyiminoacetamide Chemical compound ON=CC(=O)NC1=CC=C(Cl)C=C1 HPTQNIZSFRLFIU-UHFFFAOYSA-N 0.000 description 1
- VZUGBLTVBZJZOE-KRWDZBQOSA-N n-[3-[(4s)-2-amino-1,4-dimethyl-6-oxo-5h-pyrimidin-4-yl]phenyl]-5-chloropyrimidine-2-carboxamide Chemical compound N1=C(N)N(C)C(=O)C[C@@]1(C)C1=CC=CC(NC(=O)C=2N=CC(Cl)=CN=2)=C1 VZUGBLTVBZJZOE-KRWDZBQOSA-N 0.000 description 1
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- UQJQVUOTMVCFHX-UHFFFAOYSA-L nabam Chemical compound [Na+].[Na+].[S-]C(=S)NCCNC([S-])=S UQJQVUOTMVCFHX-UHFFFAOYSA-L 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
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- PMCVMORKVPSKHZ-UHFFFAOYSA-N oxydemeton-methyl Chemical compound CCS(=O)CCSP(=O)(OC)OC PMCVMORKVPSKHZ-UHFFFAOYSA-N 0.000 description 1
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- 239000003208 petroleum Substances 0.000 description 1
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 1
- 230000037039 plant physiology Effects 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- AQHNPKFHIGUTLK-UHFFFAOYSA-N propyl 3-ethyl-5-(ethylcarbamoylamino)-1,2-oxazole-4-carboxylate Chemical compound CCCOC(=O)C=1C(CC)=NOC=1NC(=O)NCC AQHNPKFHIGUTLK-UHFFFAOYSA-N 0.000 description 1
- UEXYLBNIDKROHC-UHFFFAOYSA-N propyl 5-(ethylcarbamoylamino)-3-methyl-1,2-oxazole-4-carboxylate Chemical compound CCCOC(=O)C=1C(C)=NOC=1NC(=O)NCC UEXYLBNIDKROHC-UHFFFAOYSA-N 0.000 description 1
- UGSWPWUBBYZFEB-UHFFFAOYSA-N propyl 5-amino-3-methyl-1,2-oxazole-4-carboxylate Chemical compound CCCOC(=O)C=1C(C)=NOC=1N UGSWPWUBBYZFEB-UHFFFAOYSA-N 0.000 description 1
- PHNUZKMIPFFYSO-UHFFFAOYSA-N propyzamide Chemical compound C#CC(C)(C)NC(=O)C1=CC(Cl)=CC(Cl)=C1 PHNUZKMIPFFYSO-UHFFFAOYSA-N 0.000 description 1
- DOYOPBSXEIZLRE-UHFFFAOYSA-N pyrrole-3-carboxylic acid Chemical compound OC(=O)C=1C=CNC=1 DOYOPBSXEIZLRE-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
-
- 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<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D261/14—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4555577 | 1977-11-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD141257A5 true DD141257A5 (de) | 1980-04-23 |
Family
ID=10437648
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD78208817A DD141257A5 (de) | 1977-11-02 | 1978-11-01 | Pestizide bzw.pflanzenwachstumsregulierende zusammensetzungen |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0002881A1 (es) |
| JP (1) | JPS5470266A (es) |
| DD (1) | DD141257A5 (es) |
| DK (1) | DK480778A (es) |
| ES (1) | ES474696A1 (es) |
| IT (1) | IT7829298A0 (es) |
| PL (1) | PL210666A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4507145A (en) * | 1980-02-19 | 1985-03-26 | Ppg Industries, Inc. | Herbicidal 3-[substituted 3- or 5-isoxazolyl]-1-4-, or 5-substituted-2-imidazolidinones |
| US4336264A (en) * | 1980-06-19 | 1982-06-22 | Eli Lilly And Company | 1-Benzoyl-3-(isoxazolyl or benzisoxazolyl)-ureas and insecticidal use thereof |
| US4529435A (en) * | 1980-11-18 | 1985-07-16 | Ppg Industries, Inc. | Herbicidally active isoxazol acetal ureas |
| JPS58194869A (ja) * | 1982-05-10 | 1983-11-12 | Sankyo Co Ltd | イソオキサゾリノン誘導体及び殺虫・殺ダニ剤 |
| US4689071A (en) * | 1983-05-05 | 1987-08-25 | Ppg Industries, Inc. | Herbicidally active 3-isoxazolyl-2-imidazolidinone derivatives |
| DE3465739D1 (de) * | 1983-06-27 | 1987-10-08 | Shell Int Research | Oxazolyl-substituted diazaheterocycles |
| DE3501723A1 (de) * | 1985-01-19 | 1986-07-24 | Bayer Ag, 5090 Leverkusen | Substituierte furazane |
| US4707180A (en) * | 1985-06-14 | 1987-11-17 | Ppg Industries, Inc. | Herbicidally active isoxazolyl-imidazolidinone derivatives |
| EP0427963B1 (de) * | 1989-11-10 | 1994-03-30 | Agrolinz Agrarchemikalien Gesellschaft M.B.H. | Verfahren zur Herstellung reiner, unsymmetrisch disubstituierter Harnstoffe |
| DE3940261A1 (de) * | 1989-12-06 | 1991-06-13 | Agrolinz Agrarchemikalien Muen | Verfahren zur herstellung reiner, unsymmetrisch disubstituierter harnstoffe |
| DE4406209A1 (de) * | 1994-02-25 | 1995-08-31 | Basf Ag | Cyanoisoxazole |
| US6297198B1 (en) | 1996-05-14 | 2001-10-02 | Syngenta Participations Ag | Isoxazole derivatives and their use as herbicides |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3547940A (en) * | 1967-10-31 | 1970-12-15 | Du Pont | Substituted ureido isoxazoles |
| US3743498A (en) * | 1967-10-31 | 1973-07-03 | Du Pont | Method of selectively controlling undesirable vegetation |
| US3917632A (en) * | 1972-06-14 | 1975-11-04 | Hoffmann La Roche | 5-Amino isoxazole from 3-amino acrylonitrile |
| JPS5031039A (es) * | 1973-07-27 | 1975-03-27 | ||
| JPS5810361B2 (ja) * | 1974-10-04 | 1983-02-25 | 塩野義製薬株式会社 | ３−アルチルイソオキサゾ−ル系除草剤 |
-
1978
- 1978-10-12 EP EP78300497A patent/EP0002881A1/en not_active Withdrawn
- 1978-10-27 DK DK480778A patent/DK480778A/da unknown
- 1978-10-31 IT IT7829298A patent/IT7829298A0/it unknown
- 1978-10-31 ES ES474696A patent/ES474696A1/es not_active Expired
- 1978-11-01 JP JP13384678A patent/JPS5470266A/ja active Pending
- 1978-11-01 DD DD78208817A patent/DD141257A5/de unknown
- 1978-11-02 PL PL21066678A patent/PL210666A1/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES474696A1 (es) | 1980-01-16 |
| JPS5470266A (en) | 1979-06-05 |
| DK480778A (da) | 1979-05-03 |
| IT7829298A0 (it) | 1978-10-31 |
| EP0002881A1 (en) | 1979-07-11 |
| PL210666A1 (es) | 1980-08-11 |
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