ZA200107811B - Pesticidal enantiomer-pure 2,4-disubstituted oxazolines. - Google Patents
Pesticidal enantiomer-pure 2,4-disubstituted oxazolines. Download PDFInfo
- Publication number
- ZA200107811B ZA200107811B ZA200107811A ZA200107811A ZA200107811B ZA 200107811 B ZA200107811 B ZA 200107811B ZA 200107811 A ZA200107811 A ZA 200107811A ZA 200107811 A ZA200107811 A ZA 200107811A ZA 200107811 B ZA200107811 B ZA 200107811B
- Authority
- ZA
- South Africa
- Prior art keywords
- spp
- enantiomer
- formula
- active ingredient
- crop protection
- Prior art date
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- 239000000049 pigment Substances 0.000 description 1
- 239000012165 plant wax Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 235000021018 plums Nutrition 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229940093429 polyethylene glycol 6000 Drugs 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 235000021039 pomes Nutrition 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 229960002957 praziquantel Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- PWYIUEFFPNVCMW-UHFFFAOYSA-N propaphos Chemical compound CCCOP(=O)(OCCC)OC1=CC=C(SC)C=C1 PWYIUEFFPNVCMW-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 229940015367 pyrethrum Drugs 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000010499 rapseed oil Substances 0.000 description 1
- 235000021013 raspberries Nutrition 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 229940080817 rotenone Drugs 0.000 description 1
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 1
- 229960000581 salicylamide Drugs 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- PYODKQIVQIVELM-UHFFFAOYSA-M sodium;2,3-bis(2-methylpropyl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 PYODKQIVQIVELM-UHFFFAOYSA-M 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 239000012439 solid excipient Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000007910 systemic administration Methods 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000002700 tablet coating Substances 0.000 description 1
- 238000009492 tablet coating Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 229940074152 thuringiensin Drugs 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 229960000323 triclabendazole Drugs 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 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
- 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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH58399 | 1999-03-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200107811B true ZA200107811B (en) | 2002-08-23 |
Family
ID=4190365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200107811A ZA200107811B (en) | 1999-03-26 | 2001-09-21 | Pesticidal enantiomer-pure 2,4-disubstituted oxazolines. |
Country Status (13)
Country | Link |
---|---|
US (1) | US20020137781A1 (de) |
EP (1) | EP1165527A1 (de) |
JP (1) | JP2002540194A (de) |
KR (1) | KR100699973B1 (de) |
CN (1) | CN1135225C (de) |
AU (1) | AU767434B2 (de) |
BR (1) | BR0009357A (de) |
CA (1) | CA2367508C (de) |
MX (1) | MXPA01009788A (de) |
NZ (1) | NZ514064A (de) |
RU (1) | RU2233838C2 (de) |
WO (1) | WO2000058291A1 (de) |
ZA (1) | ZA200107811B (de) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2403408B (en) * | 2003-07-03 | 2007-09-19 | Michael Hilary Burke | Process for preparing a stable anthelmintic suspension formulation |
AU2006286809B2 (en) * | 2005-08-29 | 2011-07-07 | Novartis Tiergesundheit Ag | Use of oxazole derivatives for controlling fish parasites |
WO2009040248A1 (en) * | 2007-09-27 | 2009-04-02 | Basf Se | Systemicity enhancers |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW440429B (en) * | 1994-08-12 | 2001-06-16 | Bayer Ag | Substituted biphenyloxazolines |
AU684674B2 (en) * | 1994-10-06 | 1997-12-18 | Bayer Aktiengesellschaft | Substituted diphenyl oxazolines |
DE4444111A1 (de) * | 1994-12-12 | 1996-06-13 | Bayer Ag | Substituierte m-Biphenyloxazolin-Derivate |
AU4243796A (en) * | 1995-01-20 | 1996-08-07 | E.I. Du Pont De Nemours And Company | Insecticidal and acaricidal oxazolines and thiazolines |
US6211214B1 (en) * | 1995-11-17 | 2001-04-03 | Bayer Aktiengesellschaft | Biphenyl ether oxazolines and their use as pest-control agents |
TW424089B (en) * | 1996-01-16 | 2001-03-01 | Du Pont | Oxazoline arthropodicides |
ZA979502B (en) * | 1996-11-18 | 1999-04-23 | Du Pont | Arthropodicidal oxazoline derivatives and processes and intermediates for the preparation thereof |
JP2001526636A (ja) * | 1997-03-05 | 2001-12-18 | バイエル・アクチエンゲゼルシヤフト | 二置換ビフェニルオキサゾリン |
DE19717228A1 (de) * | 1997-04-24 | 1998-10-29 | Bayer Ag | Substituierte Oxazolin-Derivate |
DE19727889A1 (de) * | 1997-07-01 | 1999-01-07 | Bayer Ag | 2-(2-Methylphenyl)-oxazoline |
CO5031296A1 (es) * | 1997-11-04 | 2001-04-27 | Novartis Ag | Derivados de azolina, compuestos que la contienen y metodo para la preparacion y aplicacion de dicho compuesto |
-
2000
- 2000-03-24 EP EP00922546A patent/EP1165527A1/de not_active Withdrawn
- 2000-03-24 CA CA2367508A patent/CA2367508C/en not_active Expired - Fee Related
- 2000-03-24 KR KR1020017012185A patent/KR100699973B1/ko not_active IP Right Cessation
- 2000-03-24 JP JP2000607994A patent/JP2002540194A/ja not_active Withdrawn
- 2000-03-24 BR BR0009357-2A patent/BR0009357A/pt not_active Application Discontinuation
- 2000-03-24 WO PCT/EP2000/002641 patent/WO2000058291A1/en active IP Right Grant
- 2000-03-24 AU AU42904/00A patent/AU767434B2/en not_active Ceased
- 2000-03-24 RU RU2001126543/04A patent/RU2233838C2/ru not_active IP Right Cessation
- 2000-03-24 NZ NZ514064A patent/NZ514064A/xx unknown
- 2000-03-24 CN CNB008055904A patent/CN1135225C/zh not_active Expired - Fee Related
- 2000-03-24 MX MXPA01009788A patent/MXPA01009788A/es not_active Application Discontinuation
-
2001
- 2001-09-21 ZA ZA200107811A patent/ZA200107811B/en unknown
- 2001-09-24 US US09/961,888 patent/US20020137781A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU767434B2 (en) | 2003-11-13 |
US20020137781A1 (en) | 2002-09-26 |
NZ514064A (en) | 2004-01-30 |
MXPA01009788A (es) | 2002-03-27 |
JP2002540194A (ja) | 2002-11-26 |
WO2000058291A1 (en) | 2000-10-05 |
CN1345313A (zh) | 2002-04-17 |
KR100699973B1 (ko) | 2007-03-27 |
CN1135225C (zh) | 2004-01-21 |
AU4290400A (en) | 2000-10-16 |
RU2233838C2 (ru) | 2004-08-10 |
KR20020008387A (ko) | 2002-01-30 |
EP1165527A1 (de) | 2002-01-02 |
BR0009357A (pt) | 2002-03-05 |
CA2367508C (en) | 2011-04-26 |
CA2367508A1 (en) | 2000-10-05 |
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