DD235554A5 - Zusammensetzung zum toeten von warmblutschaedlingen - Google Patents

Zusammensetzung zum toeten von warmblutschaedlingen Download PDF

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Publication number: DD235554A5
Authority: DD; German Democratic Republic
Prior art keywords: group; item; straight; carbon atoms; acid addition
Prior art date: 1984-02-08

Application number

DD85273149A

Other languages

German (de)

English (en)

Inventor

Leslie R Hatton

Original Assignee

��@�K@��@��Kk��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-02-08

Filing date

1985-02-08

Publication date

1986-05-14

1984-02-08 Priority claimed from GB848403362A external-priority patent/GB8403362D0/en

1984-12-12 Priority claimed from GB848431375A external-priority patent/GB8431375D0/en

1985-02-08 Application filed by ��@�K@��@��Kk�� filed Critical ��@�K@��@��Kk��

1986-05-14 Publication of DD235554A5 publication Critical patent/DD235554A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 53
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239000002253 acid Substances 0.000 claims abstract description 48
150000003839 salts Chemical class 0.000 claims abstract description 44
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125000004432 carbon atom Chemical group C* 0.000 claims abstract description 28
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241000400611 Eucalyptus deanei Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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 description 1
206010061217 Infestation Diseases 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
238000003820 Medium-pressure liquid chromatography Methods 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
BUIQRTDBPCHRIR-UHFFFAOYSA-L O[Cr](Cl)(=O)=O Chemical compound O[Cr](Cl)(=O)=O BUIQRTDBPCHRIR-UHFFFAOYSA-L 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
QPFYXYFORQJZEC-FOCLMDBBSA-N Phenazopyridine Chemical compound NC1=NC(N)=CC=C1\N=N\C1=CC=CC=C1 QPFYXYFORQJZEC-FOCLMDBBSA-N 0.000 description 1
206010035148 Plague Diseases 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
206010039897 Sedation Diseases 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
XCYPSDGZVGBSEM-UHFFFAOYSA-N [2-[1-[3-[3,5-bis(trifluoromethyl)phenyl]prop-2-ynyl]piperidin-4-yl]-2-methylpropyl] methanesulfonate Chemical compound C1CC(C(C)(COS(C)(=O)=O)C)CCN1CC#CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 XCYPSDGZVGBSEM-UHFFFAOYSA-N 0.000 description 1
WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
239000012346 acetyl chloride Substances 0.000 description 1
231100000460 acute oral toxicity Toxicity 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000002152 aqueous-organic solution Substances 0.000 description 1
125000005279 aryl sulfonyloxy group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
235000015278 beef Nutrition 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000037396 body weight Effects 0.000 description 1
235000008429 bread Nutrition 0.000 description 1
235000012970 cakes Nutrition 0.000 description 1
125000001589 carboacyl group Chemical group 0.000 description 1
239000004464 cereal grain Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
229940045803 cuprous chloride Drugs 0.000 description 1
230000006378 damage Effects 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
238000010828 elution Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000008029 eradication Effects 0.000 description 1
239000003925 fat Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
235000012631 food intake Nutrition 0.000 description 1
FATAVLOOLIRUNA-UHFFFAOYSA-N formylmethyl Chemical group [CH2]C=O FATAVLOOLIRUNA-UHFFFAOYSA-N 0.000 description 1
239000012458 free base Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
150000002443 hydroxylamines Chemical class 0.000 description 1
239000011630 iodine Substances 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
231100000225 lethality Toxicity 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000010907 mechanical stirring Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
239000004533 oil dispersion Substances 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000011087 paperboard Substances 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
239000006187 pill Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229910003446 platinum oxide Inorganic materials 0.000 description 1
235000015277 pork Nutrition 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229940070891 pyridium Drugs 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000036280 sedation Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000012258 stirred mixture Substances 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
125000005424 tosyloxy group Chemical group S(=O)(=O)(C1=CC=C(C)C=C1)O* 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
- C07D211/28—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms to which a second hetero atom is attached
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Hydrogenated Pyridines (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD85273149A 1984-02-08 1985-02-08 Zusammensetzung zum toeten von warmblutschaedlingen DD235554A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB848403362A GB8403362D0 (en)	1984-02-08	1984-02-08	Compositions of matter
GB848431375A GB8431375D0 (en)	1984-12-12	1984-12-12	Compositions of matter

Publications (1)

Publication Number	Publication Date
DD235554A5 true DD235554A5 (de)	1986-05-14

Family

ID=26287301

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85273149A DD235554A5 (de)	1984-02-08	1985-02-08	Zusammensetzung zum toeten von warmblutschaedlingen

Country Status (15)

Country	Link
US (1)	US4871748A (fr)
AU (1)	AU588795B2 (fr)
BE (1)	BE901681A (fr)
BR (1)	BR8500554A (fr)
CA (1)	CA1280420C (fr)
CH (1)	CH665836A5 (fr)
DD (1)	DD235554A5 (fr)
DE (1)	DE3504412A1 (fr)
DK (1)	DK54085A (fr)
FR (1)	FR2559149B1 (fr)
GB (1)	GB2153827B (fr)
IL (1)	IL74231A (fr)
IT (1)	IT1183330B (fr)
LU (1)	LU85762A1 (fr)
NL (1)	NL8500347A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5252586A (en) *	1990-09-28	1993-10-12	The Du Pont Merck Pharmaceutical Company	Ether derivatives of alkyl piperidines and pyrrolidines as antipsychotic agents
ES2154570B1 (es) *	1998-10-23	2001-10-16	Almirall Prodesfarma Sa	Nuevos compuestos de peperidina y su uso como raticidas.
ATE327673T1 (de) *	2001-08-23	2006-06-15	Bayer Cropscience Sa	Substituierte propargylamine

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1483709A (fr) *	1962-07-11	1967-06-09		Composés basiques se rattachant au butane et leur préparation
GB1055548A (en) *	1965-08-23	1967-01-18	Acraf	New substituted 1-aryl-3-aminopropynes and process for their preparation
US4180574A (en) *	1978-12-26	1979-12-25	Abbott Laboratories	Certain ovicidal piperazines
US4285957A (en) *	1979-04-10	1981-08-25	Richardson-Merrell Inc.	1-Piperidine-alkanol derivatives, pharmaceutical compositions thereof, and method of use thereof
ZA813127B (en) *	1980-05-13	1982-05-26	May & Baker Ltd	A new phenylpropargylamine derivative
US4634699A (en) *	1983-11-30	1987-01-06	Burroughs Wellcome Co.	Branched chain phenothiazine

1985
- 1985-01-23 US US06/693,729 patent/US4871748A/en not_active Expired - Fee Related
- 1985-01-31 FR FR8501530A patent/FR2559149B1/fr not_active Expired
- 1985-02-03 IL IL74231A patent/IL74231A/xx unknown
- 1985-02-06 CA CA000473676A patent/CA1280420C/fr not_active Expired - Fee Related
- 1985-02-06 AU AU38487/85A patent/AU588795B2/en not_active Ceased
- 1985-02-06 LU LU85762A patent/LU85762A1/fr unknown
- 1985-02-06 DK DK54085A patent/DK54085A/da not_active Application Discontinuation
- 1985-02-07 BE BE0/214473A patent/BE901681A/fr not_active IP Right Cessation
- 1985-02-07 BR BR8500554A patent/BR8500554A/pt unknown
- 1985-02-07 CH CH562/85A patent/CH665836A5/fr not_active IP Right Cessation
- 1985-02-07 NL NL8500347A patent/NL8500347A/nl not_active Application Discontinuation
- 1985-02-07 GB GB08503123A patent/GB2153827B/en not_active Expired
- 1985-02-08 DD DD85273149A patent/DD235554A5/de unknown
- 1985-02-08 DE DE19853504412 patent/DE3504412A1/de not_active Withdrawn
- 1985-02-08 IT IT19442/85A patent/IT1183330B/it active

Also Published As

Publication number	Publication date
CA1280420C (fr)	1991-02-19
LU85762A1 (fr)	1986-09-02
AU588795B2 (en)	1989-09-28
IT1183330B (it)	1987-10-22
IL74231A (en)	1988-10-31
GB8503123D0 (en)	1985-03-13
BE901681A (fr)	1985-08-07
GB2153827A (en)	1985-08-29
BR8500554A (pt)	1985-09-24
DE3504412A1 (de)	1985-08-08
CH665836A5 (fr)	1988-06-15
US4871748A (en)	1989-10-03
GB2153827B (en)	1987-10-21
FR2559149B1 (fr)	1989-11-24
IT8519442A0 (it)	1985-02-08
AU3848785A (en)	1985-08-15
IL74231A0 (en)	1985-05-31
DK54085A (da)	1985-08-09
FR2559149A1 (fr)	1985-08-09
DK54085D0 (da)	1985-02-06
NL8500347A (nl)	1985-09-02

Legal Events

Date	Code	Title	Description
1986-05-14	A5	Published as prov. exclusive patent

Publication	Publication Date	Title
DE69217085T2 (de)	1997-05-28	Insekttötende phenylhydrazin-derivate
DE2653189C2 (de)	1985-02-14	Cyclopropanverbindungen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Insektizide
DE2603877C2 (de)	1985-03-07	Oxadiazolinonverbindungen, ihre Herstellung und sie enthaltendes Mittel
AT389800B (de)	1990-01-25	Fungizides mittel
DE3604781A1 (de)	1987-08-27	Neue silane, verfahren zu ihrer herstellung und diese verbindungen enthaltende einsektizide mittel
CH622784A5 (en)	1981-04-30	Process for the preparation of 1,4-diphenyl-3-pyrazolin-5-ones
DE1811409A1 (de)	1970-06-18	Mittel zur Bekaempfung von Insekten,Milben,Hasenartigen und Nagetieren
DE1667979A1 (de)	1971-07-15	Schaedlingsbekaempfungsmittel,die bestimmte Benzodioxole enthalten,sowie Verfahren zu deren Herstellung
US4347252A (en)	1982-08-31	Rodenticidal 1-(3,5-bistrifluoromethylphenyl)-3-(4-t-butylpiperidino)prop-1-yne
DE2707801A1 (de)	1977-09-01	Bekaempfung von insekten und milben mit hilfe von 1-carbamyl-4h-1,2,4-triazolin-5-onen und -thionen
DD235554A5 (de)	1986-05-14	Zusammensetzung zum toeten von warmblutschaedlingen
EP0007089A1 (fr)	1980-01-23	Acylanilides à activité herbicide et fungicide, procédé pour leur préparation et leur utilisation
AT388916B (de)	1989-09-25	Verfahren zur herstellung von neuen phenylpropargylaminderivaten und deren saeureadditionssalzen
DE2361463A1 (de)	1974-06-12	Herbicid-kombination
DE2524578A1 (de)	1975-12-11	Barbitursaeurederivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE2307519A1 (de)	1973-12-06	Phosphorylierte benzimidazole
DE2034695A1 (de)	1971-01-28	Substituierte 3,4 Dihydro 1H-2,1,3benzothiadiazino 2,2 dioxide mit pestizider Wirkung
EP0299313B1 (fr)	1991-07-03	Pesticide à base de dérivés du nitrile de l'acide 2,3-diaminomaléique
DE1695231B1 (de)	1972-05-04	3-Carbalkoxy-4-hydroxy-chinolinderivate
DE1642331A1 (de)	1971-11-18	Herbizide Zubereitungen
EP0584653A1 (fr)	1994-03-02	Procédé de lutte contre les blattes et compostions pour combattre les luttes
DE2336827A1 (de)	1974-01-31	Delta hoch 2 -1,2,4-triazolin-1- oder -4-yl-methyl-phosphorverbindungen und deren verwendung als pesticide
AT324045B (de)	1975-08-11	Insektizide und akarizide zusammensetzungen
DE2409686A1 (de)	1974-10-10	3-pyridylmethylarylharnstoffe
DE1002341B (de)	1957-02-14	Verfahren zur Herstellung halogenierter Bicyclo-[2,2,1]-heptene-(2)