KR930019657A - 디옥솔란 유도체 및 이를 활성성분으로 함유하는 살충제 조성물 - Google Patents

디옥솔란 유도체 및 이를 활성성분으로 함유하는 살충제 조성물 Download PDF

Info

Publication number: KR930019657A
Authority: KR; South Korea
Prior art keywords: chloro; compound; formula; dioxolane; alkyl
Prior art date: 1992-03-02
Legal status (The legal status 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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

KR1019930002937A

Other languages

English (en)

Korean (ko)

Inventor

카레르 프리드리히

Original Assignee

베르너 발데크

시바-가이기 아게

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.)

1992-03-02

Filing date

1993-02-25

Publication date

1993-10-18

1993-02-25 Application filed by 베르너 발데크, 시바-가이기 아게 filed Critical 베르너 발데크

1993-10-18 Publication of KR930019657A publication Critical patent/KR930019657A/ko

Status Withdrawn legal-status Critical Current

Links

239000004480 active ingredient Substances 0.000 title claims abstract 4
239000000203 mixture Substances 0.000 title claims 7
239000000575 pesticide Substances 0.000 title claims 3
150000004862 dioxolanes Chemical class 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract 29
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract 11
229910052801 chlorine Inorganic materials 0.000 claims abstract 11
239000000460 chlorine Substances 0.000 claims abstract 11
-1 halo-C1-C3-alkyl Chemical group 0.000 claims abstract 8
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 7
229910052731 fluorine Inorganic materials 0.000 claims abstract 7
239000011737 fluorine Substances 0.000 claims abstract 7
229910052739 hydrogen Inorganic materials 0.000 claims abstract 7
239000001257 hydrogen Substances 0.000 claims abstract 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract 5
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract 5
229910052794 bromium Inorganic materials 0.000 claims abstract 5
229910052799 carbon Inorganic materials 0.000 claims abstract 5
125000004432 carbon atom Chemical group C* 0.000 claims abstract 4
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims abstract 4
229910052760 oxygen Inorganic materials 0.000 claims abstract 4
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims abstract 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract 2
150000001721 carbon Chemical group 0.000 claims abstract 2
125000004430 oxygen atom Chemical group O* 0.000 claims abstract 2
229910052717 sulfur Inorganic materials 0.000 claims abstract 2
241000607479 Yersinia pestis Species 0.000 claims 7
238000000034 method Methods 0.000 claims 6
241000238631 Hexapoda Species 0.000 claims 5
150000003254 radicals Chemical class 0.000 claims 4
241000238876 Acari Species 0.000 claims 3
241001465754 Metazoa Species 0.000 claims 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
239000003377 acid catalyst Substances 0.000 claims 2
239000002671 adjuvant Substances 0.000 claims 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
239000001301 oxygen Substances 0.000 claims 2
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
JXXYLGPGCXLHKE-UHFFFAOYSA-N 4-[(2-chloro-4-phenoxyphenoxy)methyl]-2-cyclopropyl-1,3-dioxolane Chemical compound C=1C=C(OCC2OC(OC2)C2CC2)C(Cl)=CC=1OC1=CC=CC=C1 JXXYLGPGCXLHKE-UHFFFAOYSA-N 0.000 claims 1
QCOAHUQNNMWNAQ-UHFFFAOYSA-N 4-[(4-benzyl-2-chlorophenoxy)methyl]-2-cyclopropyl-1,3-dioxolane Chemical compound C=1C=C(OCC2OC(OC2)C2CC2)C(Cl)=CC=1CC1=CC=CC=C1 QCOAHUQNNMWNAQ-UHFFFAOYSA-N 0.000 claims 1
OKBLRANODSOJDV-UHFFFAOYSA-N 4-[(4-benzyl-2-chlorophenoxy)methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=CC=C1 OKBLRANODSOJDV-UHFFFAOYSA-N 0.000 claims 1
JEZCBLRLSOPSTR-UHFFFAOYSA-N 4-[(4-benzyl-2-chlorophenoxy)methyl]-2-propan-2-yl-1,3-dioxolane Chemical compound O1C(C(C)C)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=CC=C1 JEZCBLRLSOPSTR-UHFFFAOYSA-N 0.000 claims 1
RZYYWCRIJWOAAM-UHFFFAOYSA-N 4-[(4-benzyl-2-chlorophenoxy)methyl]-2-propyl-1,3-dioxolane Chemical compound O1C(CCC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=CC=C1 RZYYWCRIJWOAAM-UHFFFAOYSA-N 0.000 claims 1
OKLYFZNRZUJQMR-UHFFFAOYSA-N 4-[[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC(F)=CC(F)=C1 OKLYFZNRZUJQMR-UHFFFAOYSA-N 0.000 claims 1
XLHKSIQNCHZZST-UHFFFAOYSA-N 4-[[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methyl]-2-propan-2-yl-1,3-dioxolane Chemical compound O1C(C(C)C)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC(F)=CC(F)=C1 XLHKSIQNCHZZST-UHFFFAOYSA-N 0.000 claims 1
JMYSKZIYJTYIMU-UHFFFAOYSA-N 4-[[2-chloro-4-(3,5-difluorophenoxy)phenoxy]methyl]-2-propyl-1,3-dioxolane Chemical compound O1C(CCC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC(F)=CC(F)=C1 JMYSKZIYJTYIMU-UHFFFAOYSA-N 0.000 claims 1
FMLCSERMNVTKPG-UHFFFAOYSA-N 4-[[2-chloro-4-(3-chloro-4-fluorophenoxy)phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=C(F)C(Cl)=C1 FMLCSERMNVTKPG-UHFFFAOYSA-N 0.000 claims 1
CWCGZJRJOFQSAW-UHFFFAOYSA-N 4-[[2-chloro-4-(3-chlorophenoxy)phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(Cl)=C1 CWCGZJRJOFQSAW-UHFFFAOYSA-N 0.000 claims 1
KYWKYGKHCHQXRH-UHFFFAOYSA-N 4-[[2-chloro-4-(3-chlorophenoxy)phenoxy]methyl]-2-propan-2-yl-1,3-dioxolane Chemical compound O1C(C(C)C)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(Cl)=C1 KYWKYGKHCHQXRH-UHFFFAOYSA-N 0.000 claims 1
CLJRHZKKQAVYQF-UHFFFAOYSA-N 4-[[2-chloro-4-(3-chlorophenoxy)phenoxy]methyl]-2-propyl-1,3-dioxolane Chemical compound O1C(CCC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(Cl)=C1 CLJRHZKKQAVYQF-UHFFFAOYSA-N 0.000 claims 1
YOJQRUZPUQZKQU-UHFFFAOYSA-N 4-[[2-chloro-4-(3-fluorophenoxy)phenoxy]methyl]-2-cyclopropyl-1,3-dioxolane Chemical compound FC1=CC=CC(OC=2C=C(Cl)C(OCC3OC(OC3)C3CC3)=CC=2)=C1 YOJQRUZPUQZKQU-UHFFFAOYSA-N 0.000 claims 1
SZPBOHTVAJYLLI-UHFFFAOYSA-N 4-[[2-chloro-4-(3-fluorophenoxy)phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(F)=C1 SZPBOHTVAJYLLI-UHFFFAOYSA-N 0.000 claims 1
YJPRALPBTCWGLH-UHFFFAOYSA-N 4-[[2-chloro-4-(3-fluorophenoxy)phenoxy]methyl]-2-propan-2-yl-1,3-dioxolane Chemical compound O1C(C(C)C)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(F)=C1 YJPRALPBTCWGLH-UHFFFAOYSA-N 0.000 claims 1
DNCFRWYKIGFJOD-UHFFFAOYSA-N 4-[[2-chloro-4-(3-fluorophenoxy)phenoxy]methyl]-2-propyl-1,3-dioxolane Chemical compound O1C(CCC)OCC1COC(C(=C1)Cl)=CC=C1OC1=CC=CC(F)=C1 DNCFRWYKIGFJOD-UHFFFAOYSA-N 0.000 claims 1
MEPDWWRFAPQNQP-UHFFFAOYSA-N 4-[[2-chloro-4-[(3,4-dichlorophenyl)methyl]phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=C(Cl)C(Cl)=C1 MEPDWWRFAPQNQP-UHFFFAOYSA-N 0.000 claims 1
NZRCMOAMXZJLBX-UHFFFAOYSA-N 4-[[2-chloro-4-[(3,5-difluorophenyl)methyl]phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC(F)=CC(F)=C1 NZRCMOAMXZJLBX-UHFFFAOYSA-N 0.000 claims 1
JLSQHRKSVSDTNA-UHFFFAOYSA-N 4-[[2-chloro-4-[(3-fluorophenyl)methyl]phenoxy]methyl]-2-ethyl-1,3-dioxolane Chemical compound O1C(CC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=CC(F)=C1 JLSQHRKSVSDTNA-UHFFFAOYSA-N 0.000 claims 1
KRYKISMTCLJOJF-UHFFFAOYSA-N 4-[[2-chloro-4-[(3-fluorophenyl)methyl]phenoxy]methyl]-2-propyl-1,3-dioxolane Chemical compound O1C(CCC)OCC1COC(C(=C1)Cl)=CC=C1CC1=CC=CC(F)=C1 KRYKISMTCLJOJF-UHFFFAOYSA-N 0.000 claims 1
241001124076 Aphididae Species 0.000 claims 1
241000233866 Fungi Species 0.000 claims 1
241000258937 Hemiptera Species 0.000 claims 1
206010061217 Infestation Diseases 0.000 claims 1
238000005253 cladding Methods 0.000 claims 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
208000015181 infectious disease Diseases 0.000 claims 1
230000009545 invasion Effects 0.000 claims 1
230000001418 larval effect Effects 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 claims 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
229920002554 vinyl polymer Polymers 0.000 claims 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 4
125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
239000003905 agrochemical Substances 0.000 abstract 1
239000011203 carbon fibre reinforced carbon Substances 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/12—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/72—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 spiro-condensed with carbocyclic rings
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/24—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
- A01N43/26—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
- A01N43/28—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/22—Radicals substituted by singly bound oxygen or sulfur atoms etherified
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings 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
- C07D317/34—Oxygen atoms

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)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Lubricants (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

KR1019930002937A 1992-03-02 1993-02-25 디옥솔란 유도체 및 이를 활성성분으로 함유하는 살충제 조성물 Withdrawn KR930019657A (ko)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH92-8/643		1992-03-02
CH64392		1992-03-02

Publications (1)

Publication Number	Publication Date
KR930019657A true KR930019657A (ko)	1993-10-18

Family

ID=4191794

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
KR1019930002937A Withdrawn KR930019657A (ko)	1992-03-02	1993-02-25	디옥솔란 유도체 및 이를 활성성분으로 함유하는 살충제 조성물

Country Status (21)

Country	Link
US (1)	US5663453A (2)
EP (1)	EP0559612B1 (2)
JP (1)	JPH0640987A (2)
KR (1)	KR930019657A (2)
CN (1)	CN1075962A (2)
AT (1)	ATE141268T1 (2)
AU (1)	AU670568B2 (2)
BR (1)	BR9300702A (2)
CA (1)	CA2090535A1 (2)
DE (1)	DE59303392D1 (2)
DK (1)	DK0559612T3 (2)
ES (1)	ES2090933T3 (2)
GR (1)	GR3020811T3 (2)
IL (1)	IL104854A (2)
MA (1)	MA22813A1 (2)
MX (1)	MX9301116A (2)
MY (1)	MY116460A (2)
NZ (1)	NZ247010A (2)
TR (1)	TR27766A (2)
TW (1)	TW231257B (2)
ZA (1)	ZA931427B (2)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE59408689D1 (de) *	1993-12-30	1999-10-07	Novartis Ag	Substituierte Phenylether als Pestizide
JP2001503034A (ja) *	1996-10-16	2001-03-06	ノバルテイス・アクチエンゲゼルシヤフト	外部寄生虫による温血動物への再寄生の予防方法
DE19846008A1 (de)	1998-10-06	2000-04-13	Bayer Ag	Phenylessigsäure-heterocyclylamide
US20060005050A1 (en) *	2004-06-10	2006-01-05	Supercom Ltd.	Tamper-free and forgery-proof passport and methods for providing same
EP2832454A1 (en)	2013-07-30	2015-02-04	Nederlandse Organisatie voor toegepast -natuurwetenschappelijk onderzoek TNO	Slot-die coating method and apparatus

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4007280A (en) *	1974-06-21	1977-02-08	Ciba-Geigy Corporation	1,4-Benzodioxan derivatives and pesticidal use thereof
US4097581A (en) *	1975-12-12	1978-06-27	Ciba-Geigy Corporation	Dioxolane derivatives
US4590282A (en) *	1984-09-24	1986-05-20	Sandoz Ltd.	Pest control agents
EP0411676B1 (de) *	1987-01-19	1994-06-15	Ciba-Geigy Ag	Substituierte Dioxanderivate
ZA913760B (en) *	1990-05-24	1992-02-26	Sumitomo Chemical Co	Pyridine derivatives,their production processes and their compounds for control of insect pests

1993
- 1993-02-19 TW TW082101160A patent/TW231257B/zh active
- 1993-02-23 DE DE59303392T patent/DE59303392D1/de not_active Expired - Fee Related
- 1993-02-23 ES ES93810125T patent/ES2090933T3/es not_active Expired - Lifetime
- 1993-02-23 AT AT93810125T patent/ATE141268T1/de not_active IP Right Cessation
- 1993-02-23 DK DK93810125.0T patent/DK0559612T3/da active
- 1993-02-23 EP EP93810125A patent/EP0559612B1/de not_active Expired - Lifetime
- 1993-02-24 MY MYPI93000325A patent/MY116460A/en unknown
- 1993-02-25 IL IL104854A patent/IL104854A/en not_active IP Right Cessation
- 1993-02-25 KR KR1019930002937A patent/KR930019657A/ko not_active Withdrawn
- 1993-02-26 NZ NZ247010A patent/NZ247010A/xx unknown
- 1993-02-26 CA CA002090535A patent/CA2090535A1/en not_active Abandoned
- 1993-03-01 BR BR9300702A patent/BR9300702A/pt not_active IP Right Cessation
- 1993-03-01 CN CN93100899A patent/CN1075962A/zh active Pending
- 1993-03-01 TR TR00163/93A patent/TR27766A/xx unknown
- 1993-03-01 MA MA23106A patent/MA22813A1/fr unknown
- 1993-03-01 AU AU33913/93A patent/AU670568B2/en not_active Ceased
- 1993-03-01 ZA ZA931427A patent/ZA931427B/xx unknown
- 1993-03-01 MX MX9301116A patent/MX9301116A/es not_active IP Right Cessation
- 1993-03-02 JP JP5066015A patent/JPH0640987A/ja active Pending
1995
- 1995-01-17 US US08/373,910 patent/US5663453A/en not_active Expired - Fee Related
1996
- 1996-08-16 GR GR960401976T patent/GR3020811T3/el unknown

Also Published As

Publication number	Publication date
AU3391393A (en)	1993-09-09
DE59303392D1 (de)	1996-09-19
ZA931427B (en)	1993-09-02
NZ247010A (en)	1995-08-28
EP0559612B1 (de)	1996-08-14
MY116460A (en)	2004-02-28
GR3020811T3 (en)	1996-11-30
DK0559612T3 (da)	1996-12-23
CA2090535A1 (en)	1993-09-03
AU670568B2 (en)	1996-07-25
IL104854A (en)	1998-06-15
TW231257B (2)	1994-10-01
CN1075962A (zh)	1993-09-08
ATE141268T1 (de)	1996-08-15
EP0559612A1 (de)	1993-09-08
BR9300702A (pt)	1993-11-16
MA22813A1 (fr)	1993-10-01
IL104854A0 (en)	1993-06-10
TR27766A (tr)	1995-08-04
US5663453A (en)	1997-09-02
JPH0640987A (ja)	1994-02-15
ES2090933T3 (es)	1996-10-16
MX9301116A (es)	1993-09-01

Legal Events

Date	Code	Title	Description
1993-02-25	PA0109	Patent application	Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19930225
1993-10-18	PG1501	Laying open of application
1997-06-04	N231	Notification of change of applicant
1997-06-04	PN2301	Change of applicant	Patent event date: 19970604 Comment text: Notification of Change of Applicant Patent event code: PN23011R01D
1998-02-25	PC1203	Withdrawal of no request for examination
1998-02-25	WITN	Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid

Publication	Publication Date	Title
SU634640A3 (ru)	1978-11-25	Гербицидна композици
KR880007500A (ko)	1988-08-27	3-페닐-5-트리플루오로메틸-1,2,4-옥사디아졸 유도체 및 그의 제조방법
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JPS62175451A (ja)	1987-08-01	殺虫活性のあるヒドラジン類
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KR880003946A (ko)	1988-06-01	Ll-f28249 화합물의 신규한 △^22-유도체 및 이를 함유한 조성물과 이의 사용방법.
JP3495056B2 (ja)	2004-02-09	殺虫組成物
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JPS63198675A (ja)	1988-08-17	置換１，３−ジオキソラン及び１，４−ジオキサン誘導体
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JPH0656611A (ja)	1994-03-01	ピラゾール系化合物とピレトリン共力剤とを含む有害生物防除剤
KR880011167A (ko)	1988-10-27	Ll-f28249 화합물의 27-할로 유도체들, 이들의 사용방법 및 이들을 포함하는 조성물
KR880003949A (ko)	1988-06-01	Ll-f28249 화합물의 신규한 △^23-유동체및 이를 함유한 조성물과 이의 사용 방법
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JPH02262582A (ja)	1990-10-25	殺虫性化合物
KR870006022A (ko)	1987-07-08	1,3,5-옥사디아진-2-온 살충제 조성물
JP2990541B2 (ja)	1999-12-13	複合殺菌殺虫剤
KR870007144A (ko)	1987-08-17	옥사디아진온
DE3134596A1 (de)	1982-08-19	Carbamatderivate, insektizide, antimilben- oder nematozide zusammensetzungen, welche diese enthalten, und verfahren zu deren herstellung
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