PL98486B1 - Srodek owadobojczy,roztoczobojczy lub nicieniobojczy - Google Patents

Srodek owadobojczy,roztoczobojczy lub nicieniobojczy Download PDF

Info

Publication number: PL98486B1
Authority: PL; Poland
Prior art keywords: cyano; radical; hours; carbon atoms; compound
Prior art date: 1975-02-14

Application number

PL1976187218A

Other languages

English (en)

Polish (pl)

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.)

1975-02-14

Filing date

1976-02-13

Publication date

1978-05-31

1976-02-13 Application filed filed Critical

1978-05-31 Publication of PL98486B1 publication Critical patent/PL98486B1/pl

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239000002917 insecticide Substances 0.000 title claims description 10
239000003795 chemical substances by application Substances 0.000 title claims description 5
150000001875 compounds Chemical class 0.000 claims description 31
125000004432 carbon atom Chemical group C* 0.000 claims description 20
230000000895 acaricidal effect Effects 0.000 claims description 8
239000004480 active ingredient Substances 0.000 claims description 8
239000000642 acaricide Substances 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
229910052717 sulfur Chemical group 0.000 claims description 4
FZTJMMWGVZSSKJ-UHFFFAOYSA-N (2-cyano-5-methylthiophen-3-yl) dimethyl phosphate Chemical compound COP(=O)(OC)OC=1C=C(C)SC=1C#N FZTJMMWGVZSSKJ-UHFFFAOYSA-N 0.000 claims description 3
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
JEVCWSUVFOYBFI-UHFFFAOYSA-N cyanyl Chemical compound N#[C] JEVCWSUVFOYBFI-UHFFFAOYSA-N 0.000 claims description 3
239000011593 sulfur Chemical group 0.000 claims description 3
IHSOUSPHWZILHU-UHFFFAOYSA-N (2-cyano-5-methoxythiophen-3-yl) dimethyl phosphate Chemical compound COC1=CC(OP(=O)(OC)OC)=C(C#N)S1 IHSOUSPHWZILHU-UHFFFAOYSA-N 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
239000000243 solution Substances 0.000 description 52
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 44
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 39
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 30
-1 alkyl radical Chemical class 0.000 description 28
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CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 26
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 26
238000012360 testing method Methods 0.000 description 26
238000004458 analytical method Methods 0.000 description 24
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238000002844 melting Methods 0.000 description 6
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ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
230000000749 insecticidal effect Effects 0.000 description 5
239000007788 liquid Substances 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
239000011591 potassium Substances 0.000 description 5
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239000000843 powder Substances 0.000 description 5
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239000013543 active substance Substances 0.000 description 4
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JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 4
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 4
229960002809 lindane Drugs 0.000 description 4
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150000003254 radicals Chemical class 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
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GIIODLNKSMCVGQ-UHFFFAOYSA-N 3-ethoxy-3-oxopropanethioic s-acid Chemical compound CCOC(=O)CC(O)=S GIIODLNKSMCVGQ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
RENMDAKOXSCIGH-UHFFFAOYSA-N Chloroacetonitrile Chemical compound ClCC#N RENMDAKOXSCIGH-UHFFFAOYSA-N 0.000 description 3
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 3
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IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 3
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CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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125000004429 atom Chemical group 0.000 description 3
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ITVPBBDAZKBMRP-UHFFFAOYSA-N chloro-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound OP(O)(Cl)=O ITVPBBDAZKBMRP-UHFFFAOYSA-N 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
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UZDLWOZHCZOAIU-UHFFFAOYSA-N 3-hydroxy-5-methylthiophene-2-carbonitrile Chemical compound CC1=CC(O)=C(C#N)S1 UZDLWOZHCZOAIU-UHFFFAOYSA-N 0.000 description 2
UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical compound CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 2
DHZOFWFPFXBMAO-UHFFFAOYSA-N 5-butoxy-3-hydroxythiophene-2-carbonitrile Chemical compound CCCCOC1=CC(O)=C(C#N)S1 DHZOFWFPFXBMAO-UHFFFAOYSA-N 0.000 description 2
JEVSLJKRRFGYFS-UHFFFAOYSA-N 5-ethylsulfanyl-3-hydroxythiophene-2-carbonitrile Chemical compound CCSC1=CC(O)=C(C#N)S1 JEVSLJKRRFGYFS-UHFFFAOYSA-N 0.000 description 2
241000238657 Blattella germanica Species 0.000 description 2
241000255579 Ceratitis capitata Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
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239000005949 Malathion Substances 0.000 description 2
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235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
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238000009835 boiling Methods 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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150000002431 hydrogen Chemical class 0.000 description 1
238000011835 investigation Methods 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
230000000974 larvacidal effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
GRKWHXNAHIMNJD-UHFFFAOYSA-N methoxysulfanyloxymethane Chemical group COSOC GRKWHXNAHIMNJD-UHFFFAOYSA-N 0.000 description 1
FELLHCNTGRGTIK-UHFFFAOYSA-N methyl 3-diethoxyphosphinothioyloxy-5-methylthiophene-2-carboxylate Chemical compound CCOP(=S)(OCC)OC=1C=C(C)SC=1C(=O)OC FELLHCNTGRGTIK-UHFFFAOYSA-N 0.000 description 1
NNPLFTBGNUKNKL-UHFFFAOYSA-N methyl 3-dimethoxyphosphoryloxy-5-methoxythiophene-2-carboxylate Chemical compound COC(=O)C=1SC(OC)=CC=1OP(=O)(OC)OC NNPLFTBGNUKNKL-UHFFFAOYSA-N 0.000 description 1
JWVGLUKLEKSZEL-UHFFFAOYSA-N methyl 3-hydroxy-5-methoxythiophene-2-carboxylate Chemical compound COC(=O)C=1SC(OC)=CC=1O JWVGLUKLEKSZEL-UHFFFAOYSA-N 0.000 description 1
PLTCMJBEOCSRII-UHFFFAOYSA-N methyl 3-hydroxy-5-methylthiophene-2-carboxylate Chemical compound COC(=O)C=1SC(C)=CC=1O PLTCMJBEOCSRII-UHFFFAOYSA-N 0.000 description 1
239000008267 milk Substances 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
UNFUYWDGSFDHCW-UHFFFAOYSA-N monochlorocyclohexane Chemical compound ClC1CCCCC1 UNFUYWDGSFDHCW-UHFFFAOYSA-N 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
230000001459 mortal effect Effects 0.000 description 1
APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical group CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
231100000194 ovacidal Toxicity 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
XUWVIABDWDTJRZ-UHFFFAOYSA-N propan-2-ylazanide Chemical compound CC(C)[NH-] XUWVIABDWDTJRZ-UHFFFAOYSA-N 0.000 description 1
SUVIGLJNEAMWEG-UHFFFAOYSA-N propane-1-thiol Chemical compound CCCS SUVIGLJNEAMWEG-UHFFFAOYSA-N 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000010076 replication Effects 0.000 description 1
229920003987 resole Polymers 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
239000010948 rhodium Substances 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000000779 smoke Substances 0.000 description 1
KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
229910001948 sodium oxide Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
238000012546 transfer Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Biochemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Life Sciences & Earth Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PL1976187218A 1975-02-14 1976-02-13 Srodek owadobojczy,roztoczobojczy lub nicieniobojczy PL98486B1 (pl)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7504628A FR2300768A1 (fr)	1975-02-14	1975-02-14	Nouveaux composes thiopeniques phosphoryles, procede de preparation et application comme pesticides

Publications (1)

Publication Number	Publication Date
PL98486B1 true PL98486B1 (pl)	1978-05-31

Family

ID=9151233

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL1976187218A PL98486B1 (pl)	1975-02-14	1976-02-13	Srodek owadobojczy,roztoczobojczy lub nicieniobojczy

Country Status (25)

Country	Link
JP (1)	JPS51105053A (fr)
BE (1)	BE838487A (fr)
BG (1)	BG25196A3 (fr)
BR (1)	BR7600876A (fr)
CA (1)	CA1074795A (fr)
CH (1)	CH610331A5 (fr)
DD (1)	DD125575A5 (fr)
DE (1)	DE2605649A1 (fr)
DK (1)	DK58376A (fr)
EG (1)	EG12442A (fr)
ES (1)	ES444618A1 (fr)
FR (1)	FR2300768A1 (fr)
GB (1)	GB1511413A (fr)
GR (1)	GR59269B (fr)
HU (1)	HU176606B (fr)
IL (1)	IL48857A (fr)
IT (1)	IT1053490B (fr)
NL (1)	NL7601489A (fr)
OA (1)	OA05248A (fr)
PH (1)	PH15203A (fr)
PL (1)	PL98486B1 (fr)
PT (1)	PT64795B (fr)
SU (1)	SU644360A3 (fr)
TR (1)	TR19251A (fr)
ZA (1)	ZA76709B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2831936A1 (de) *	1978-07-20	1980-02-07	Basf Ag	Thienylmethyl-phosphorsaeureester
JPS6058918B2 (ja) *	1980-01-22	1985-12-23	宇部興産株式会社	チオフエン誘導体および農園芸用殺菌剤
US4454131A (en) *	1982-04-30	1984-06-12	Ube Industries, Ltd.	Thiophene derivatives
WO2010101967A2 (fr) *	2009-03-04	2010-09-10	Idenix Pharmaceuticals, Inc.	Inhibiteurs de phosphothiophène et phosphothiazole vhc polymérase

1975
- 1975-02-14 FR FR7504628A patent/FR2300768A1/fr active Granted
1976
- 1976-01-16 IL IL48857A patent/IL48857A/xx unknown
- 1976-01-26 ES ES444618A patent/ES444618A1/es not_active Expired
- 1976-01-28 BG BG032211A patent/BG25196A3/xx unknown
- 1976-02-05 CA CA245,098A patent/CA1074795A/fr not_active Expired
- 1976-02-06 ZA ZA760709A patent/ZA76709B/xx unknown
- 1976-02-09 PH PH18068A patent/PH15203A/en unknown
- 1976-02-10 SU SU762318651A patent/SU644360A3/ru active
- 1976-02-10 EG EG66/76A patent/EG12442A/xx active
- 1976-02-12 DE DE19762605649 patent/DE2605649A1/de not_active Withdrawn
- 1976-02-12 BE BE164261A patent/BE838487A/fr unknown
- 1976-02-12 BR BR7600876A patent/BR7600876A/pt unknown
- 1976-02-12 DD DD191215A patent/DD125575A5/xx unknown
- 1976-02-13 IT IT48103/76A patent/IT1053490B/it active
- 1976-02-13 NL NL7601489A patent/NL7601489A/xx not_active Application Discontinuation
- 1976-02-13 GB GB5698/76A patent/GB1511413A/en not_active Expired
- 1976-02-13 HU HU76RO878A patent/HU176606B/hu unknown
- 1976-02-13 JP JP51014121A patent/JPS51105053A/ja active Pending
- 1976-02-13 DK DK58376*#A patent/DK58376A/da unknown
- 1976-02-13 GR GR50050A patent/GR59269B/el unknown
- 1976-02-13 CH CH181076A patent/CH610331A5/xx not_active IP Right Cessation
- 1976-02-13 PT PT64795A patent/PT64795B/fr unknown
- 1976-02-13 PL PL1976187218A patent/PL98486B1/pl unknown
- 1976-02-13 TR TR19251A patent/TR19251A/xx unknown
- 1976-02-14 OA OA55742A patent/OA05248A/fr unknown

Also Published As

Publication number	Publication date
DE2605649A1 (de)	1976-08-26
GB1511413A (en)	1978-05-17
PT64795B (fr)	1978-02-06
FR2300768A1 (fr)	1976-09-10
IL48857A (en)	1978-06-15
BG25196A3 (en)	1978-08-10
NL7601489A (nl)	1976-08-17
ZA76709B (en)	1977-03-30
GR59269B (en)	1977-12-05
EG12442A (en)	1981-03-31
BR7600876A (pt)	1976-09-14
HU176606B (en)	1981-03-28
DK58376A (da)	1976-08-15
IT1053490B (it)	1981-08-31
IL48857A0 (en)	1976-03-31
ES444618A1 (es)	1977-10-01
JPS51105053A (fr)	1976-09-17
PT64795A (fr)	1976-03-01
TR19251A (tr)	1978-08-15
CA1074795A (fr)	1980-04-01
PH15203A (en)	1982-09-17
DD125575A5 (fr)	1977-05-04
FR2300768B1 (fr)	1977-07-22
AU1110476A (en)	1977-08-18
CH610331A5 (en)	1979-04-12
OA05248A (fr)	1981-02-28
BE838487A (fr)	1976-08-12
SU644360A3 (ru)	1979-01-25

Publication	Publication Date	Title
DE69324552T4 (de)	2006-05-04	N'-substituierte-N,N'Diacylhydrazin-Insektizide
DE2813341C2 (de)	1983-04-28	2-Phenyl-1,3-Cyclohexandion-Derivate, ihre Herstellung und diese enthaltende Mitizide und Herbizide
PL86963B1 (fr)	1976-06-30
PL98486B1 (pl)	1978-05-31	Srodek owadobojczy,roztoczobojczy lub nicieniobojczy
EP0102062B1 (fr)	1988-11-23	1,3-Dithianes, leur préparation et emploi
PL105939B1 (pl)	1979-11-30	Srodek owadobojczy i roztoczobojczy
PL95242B1 (fr)	1977-09-30
US4473562A (en)	1984-09-25	Pesticidal O-(N-alkoxy-aliphatic hydroxamate)-phosphorus esters and thioesters
SU664530A3 (ru)	1979-05-25	Инсектоакарицидонематоцидное средство
DE2131734A1 (de)	1972-01-27	Neue organische Phosphorverbindungen,Verfahren zu ihrer Herstellung und Verwendung zur Bekaempfung tierischer und pflanzlicher Schaedlinge
KR102889687B1 (ko)	2025-11-21	작물보호제용 신규 화합물
US4086239A (en)	1978-04-25	Thiazole bis-phosphates and phosphonates, intermediates, and insecticidal compositions and methods
KR870000643B1 (ko)	1987-04-03	옥심포스페이트 화합물의 제조방법
US3206357A (en)	1965-09-14	Aminoaryltriazene pesticide
US4155996A (en)	1979-05-22	3-(Phosphoryloxy) and (phosphonyloxy)-thiophenes
CA1037049A (fr)	1978-08-22	Esters oximidophosphoriques d'acide succinique
CH636361A5 (de)	1983-05-31	Einen isoxazolinonring enthaltende mono- und dithiophosphorsaeureester.
CA1078399A (fr)	1980-05-27	Derives phosphoreux de thiophene a activite insecticide
DK142083B (da)	1980-08-25	Pyrimidinyl (thiono) (thiol)-phosphor (phosphon)-syreestere med insecticid og acaricid virkning
US4104375A (en)	1978-08-01	Isoxazole phosphates and phosphonates
KR100769708B1 (ko)	2007-10-23	살충활성을 갖는 설포닐 나프토퀴논류 화합물들의유기합성방법과 살충제 이용 기술
US4478832A (en)	1984-10-23	Pesticidal O-(N-alkoxy-substituted-benzimidoyl)-phosphorus esters and thioesters
US3935212A (en)	1976-01-27	Pesticidal substituted 2-hydroxylaminopyrimidinyl phosphorus esters
JP2673175B2 (ja)	1997-11-05	ナフトキノン系化合物、それを含む殺ダニ剤およびダニ類を防除する方法
US4066783A (en)	1978-01-03	Insecticidal and acaricidal metal halide complexes of 4-cyano-2,2-dimethylbutyraldoxime-N-methylcarbamate