DD256643A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

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Publication number: DD256643A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; formula; alkyl; propyl; butyl
Prior art date: 1986-02-18

Application number

DD87299966A

Other languages

German (de)

English (en)

Inventor

Fritz Maurer

Bernhard Homeyer

Paul Reinecke

Original Assignee

��@��k��

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.)

1986-02-18

Filing date

1987-02-17

Publication date

1988-05-18

1987-02-17 Application filed by ��@��k�� filed Critical ��@��k��

1988-05-18 Publication of DD256643A5 publication Critical patent/DD256643A5/de

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-1 6-oxo-pyrimidinyl (thiono)-phosphate Chemical compound 0.000 claims abstract description 56
125000000217 alkyl group Chemical group 0.000 claims abstract description 31
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 19
239000001257 hydrogen Substances 0.000 claims abstract description 18
150000002431 hydrogen Chemical group 0.000 claims abstract description 14
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 11
125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 9
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 7
125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 7
125000003709 fluoroalkyl group Chemical group 0.000 claims abstract description 7
239000001301 oxygen Substances 0.000 claims abstract description 7
229910052760 oxygen Inorganic materials 0.000 claims abstract description 7
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 5
229910052717 sulfur Chemical group 0.000 claims description 10
239000011593 sulfur Chemical group 0.000 claims description 10
239000000575 pesticide Substances 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 abstract description 9
229910052736 halogen Inorganic materials 0.000 abstract description 8
150000002367 halogens Chemical group 0.000 abstract description 8
239000005864 Sulphur Chemical group 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 48
125000004432 carbon atom Chemical group C* 0.000 description 31
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
239000000460 chlorine Chemical group 0.000 description 19
238000000034 method Methods 0.000 description 19
239000000203 mixture Substances 0.000 description 18
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 15
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 14
229910052801 chlorine Inorganic materials 0.000 description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 14
239000002904 solvent Substances 0.000 description 14
238000009472 formulation Methods 0.000 description 13
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
238000002360 preparation method Methods 0.000 description 11
239000002689 soil Substances 0.000 description 11
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 10
241000196324 Embryophyta Species 0.000 description 10
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 10
229910052794 bromium Inorganic materials 0.000 description 10
125000001153 fluoro group Chemical group F* 0.000 description 10
239000007858 starting material Substances 0.000 description 10
238000012360 testing method Methods 0.000 description 10
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 9
239000011737 fluorine Substances 0.000 description 9
229910052731 fluorine Inorganic materials 0.000 description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
241000238631 Hexapoda Species 0.000 description 8
239000004480 active ingredient Substances 0.000 description 8
241000607479 Yersinia pestis Species 0.000 description 7
239000003995 emulsifying agent Substances 0.000 description 7
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 7
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 6
239000000370 acceptor Substances 0.000 description 6
239000002917 insecticide Substances 0.000 description 6
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical group CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
239000004606 Fillers/Extenders Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000000969 carrier Substances 0.000 description 4
201000010099 disease Diseases 0.000 description 4
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
239000000417 fungicide Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
150000004820 halides Chemical class 0.000 description 4
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
DUFGYCAXVIUXIP-UHFFFAOYSA-N 4,6-dihydroxypyrimidine Chemical class OC1=CC(O)=NC=N1 DUFGYCAXVIUXIP-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
241000228453 Pyrenophora Species 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000000895 acaricidal effect Effects 0.000 description 3
239000000642 acaricide Substances 0.000 description 3
239000013543 active substance Substances 0.000 description 3
150000001350 alkyl halides Chemical class 0.000 description 3
125000004093 cyano group Chemical group *C#N 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
239000007788 liquid Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
239000012074 organic phase Substances 0.000 description 3
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
239000007787 solid Substances 0.000 description 3
241000894007 species Species 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
241000239223 Arachnida Species 0.000 description 2
241001480061 Blumeria graminis Species 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000371644 Curvularia ravenelii Species 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
241000084475 Delia antiqua Species 0.000 description 2
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
241000221785 Erysiphales Species 0.000 description 2
241000221787 Erysiphe Species 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
206010061217 Infestation Diseases 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000736122 Parastagonospora nodorum Species 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
241001281802 Pseudoperonospora Species 0.000 description 2
241001481703 Rhipicephalus <genus> Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
239000003513 alkali Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
150000008051 alkyl sulfates Chemical class 0.000 description 2
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
239000000920 calcium hydroxide Substances 0.000 description 2
229910001861 calcium hydroxide Inorganic materials 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
150000008050 dialkyl sulfates Chemical class 0.000 description 2
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000003814 drug Substances 0.000 description 2
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230000000855 fungicidal effect Effects 0.000 description 2
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150000002576 ketones Chemical class 0.000 description 2
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125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
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UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
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GILIYJDBJZWGBG-UHFFFAOYSA-N 1,1,1-trifluoropropan-2-ol Chemical compound CC(O)C(F)(F)F GILIYJDBJZWGBG-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
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SBMLWWSJDCBQJR-UHFFFAOYSA-N 2,3-diethyl-6-hydroxypyrimidin-4-one Chemical compound CCC1=NC(O)=CC(=O)N1CC SBMLWWSJDCBQJR-UHFFFAOYSA-N 0.000 description 1
HDBGBTNNPRCVND-UHFFFAOYSA-N 3,3,3-trifluoropropan-1-ol Chemical compound OCCC(F)(F)F HDBGBTNNPRCVND-UHFFFAOYSA-N 0.000 description 1
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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
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
- 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
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Saccharide Compounds (AREA)
Cephalosporin Compounds (AREA)

DD87299966A 1986-02-18 1987-02-17 Schaedlingsbekaempfungsmittel DD256643A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19863605002 DE3605002A1 (de)	1986-02-18	1986-02-18	Phosphorsaeureester

Publications (1)

Publication Number	Publication Date
DD256643A5 true DD256643A5 (de)	1988-05-18

Family

ID=6294291

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD87299966A DD256643A5 (de)	1986-02-18	1987-02-17	Schaedlingsbekaempfungsmittel

Country Status (13)

Country	Link
US (1)	US4771040A (ko)
EP (1)	EP0234356B1 (ko)
JP (1)	JPS62192392A (ko)
KR (1)	KR870007943A (ko)
AT (1)	ATE44960T1 (ko)
AU (1)	AU6916687A (ko)
BR (1)	BR8700710A (ko)
DD (1)	DD256643A5 (ko)
DE (2)	DE3605002A1 (ko)
DK (1)	DK79587A (ko)
HU (1)	HUT45541A (ko)
IL (1)	IL81589A0 (ko)
ZA (1)	ZA871131B (ko)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5453414A (en) *	1993-05-20	1995-09-26	Rohm And Haas Company	2-arylpyrimidines and herbicidal use thereof
US5300477A (en) *	1992-07-17	1994-04-05	Rohm And Haas Company	2-arylpyrimidines and herbicidal use thereof
US5726124A (en) *	1992-07-17	1998-03-10	Rohm And Haas Company	2-arylpyrimidines and herbicidal use thereof
US5629264A (en) *	1995-03-23	1997-05-13	Rohm And Haas Company	2-aryl-5,6-dihydropyrimidinones and herbicidal use thereof
US20030225075A1 (en) *	2002-04-10	2003-12-04	Orchid Chemicals & Pharmaceuticals Limited	Novel pyrimidone derivatives
DE60336735D1 (de) *	2002-07-22	2011-05-26	Orchid Res Lab Ltd	Neue biologischaktive molekü le
WO2007000655A2 (en) *	2005-06-28	2007-01-04	Orchid Research Laboratories Limited	Novel pyrazolopyrimidinone derivatives

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1369062A (fr) *	1962-08-24	1964-08-07	Bayer Ag	Nouvelles compositions insecticides et acaricides et leur procédé de fabrication
DE2630054A1 (de) *	1976-07-03	1978-01-12	Bayer Ag	6-oxo-pyrimidinyl(thiono)(thiol)- phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
DE2722402A1 (de) *	1977-05-17	1978-11-30	Bayer Ag	1-phenyl-6-oxo-pyrimidinyl(thiono) (thiol)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
US4575499A (en) *	1982-11-22	1986-03-11	The Dow Chemical Company	Phosphorus derivatives of 4-pyrimidinols
DE3317824A1 (de) *	1983-05-17	1984-11-22	Bayer Ag, 5090 Leverkusen	Phosphorsaeureester
DE3445465A1 (de) *	1984-12-13	1986-06-19	Bayer Ag, 5090 Leverkusen	Pyrimidinyl-thionophosphorsaeureester
DE3527861A1 (de) *	1985-08-02	1987-02-05	Bayer Ag	Phosphorsaeureester

1986
- 1986-02-18 DE DE19863605002 patent/DE3605002A1/de not_active Withdrawn
1987
- 1987-02-05 EP EP87101560A patent/EP0234356B1/de not_active Expired
- 1987-02-05 AT AT87101560T patent/ATE44960T1/de not_active IP Right Cessation
- 1987-02-05 DE DE8787101560T patent/DE3760363D1/de not_active Expired
- 1987-02-10 US US07/013,081 patent/US4771040A/en not_active Expired - Fee Related
- 1987-02-11 KR KR870001108A patent/KR870007943A/ko not_active Withdrawn
- 1987-02-11 AU AU69166/87A patent/AU6916687A/en not_active Abandoned
- 1987-02-16 IL IL81589A patent/IL81589A0/xx unknown
- 1987-02-16 JP JP62031650A patent/JPS62192392A/ja active Pending
- 1987-02-17 DK DK079587A patent/DK79587A/da not_active Application Discontinuation
- 1987-02-17 HU HU87617A patent/HUT45541A/hu unknown
- 1987-02-17 BR BR8700710A patent/BR8700710A/pt unknown
- 1987-02-17 DD DD87299966A patent/DD256643A5/de unknown
- 1987-02-17 ZA ZA871131A patent/ZA871131B/xx unknown

Also Published As

Publication number	Publication date
ZA871131B (en)	1987-08-11
BR8700710A (pt)	1987-12-22
JPS62192392A (ja)	1987-08-22
DE3760363D1 (en)	1989-08-31
AU6916687A (en)	1987-08-20
EP0234356B1 (de)	1989-07-26
US4771040A (en)	1988-09-13
DK79587A (da)	1987-08-19
DK79587D0 (da)	1987-02-17
DE3605002A1 (de)	1987-08-20
EP0234356A1 (de)	1987-09-02
KR870007943A (ko)	1987-09-23
IL81589A0 (en)	1987-09-16
ATE44960T1 (de)	1989-08-15
HUT45541A (en)	1988-07-28

Publication	Publication Date	Title
DD145998A5 (de)	1981-01-21	Insektizide,akarizide und nematizide mittel
DE3317824A1 (de)	1984-11-22	Phosphorsaeureester
DE2839270A1 (de)	1980-03-20	N,n-dimethyl-o-pyrazolyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0234356B1 (de)	1989-07-26	Phosphorsäureester
EP0276406A1 (de)	1988-08-03	Substituierte 4-Amino-pyrimidine
EP0215235B1 (de)	1989-01-25	Phosphorsäureester
EP0361185B1 (de)	1994-06-22	Substituierte 2-(Halogenmethylthio)-pyrimidin-Derivate
DE3126390A1 (de)	1983-01-13	S-azolyl-methyl-di(tri)-thiophosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
EP0073912B1 (de)	1985-03-20	Oxo-chinazolin-(thiono)-phosphor(phosphon)-säureester bzw.esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE3445465A1 (de)	1986-06-19	Pyrimidinyl-thionophosphorsaeureester
EP0658562A1 (de)	1995-06-21	Phosphorsäure-Derivate als Schäblingsbekämpfungsmittel
EP0655999A1 (de)	1995-06-07	1,2,4-dithiazolium-iodide und ihre verwendung als schädlingsbekämpfungsmittel
DE2830766A1 (de)	1980-01-31	2-cyclopropyl-pyrimidin(4)yl-(thiono) (thiol)-phosphor-(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
DE3110595A1 (de)	1982-10-21	Phosphor (phosphon)-saeureesteramide, ihre herstellung und verwendung
EP0305837A2 (de)	1989-03-08	Thionophosphonsäureester
EP0391131A2 (de)	1990-10-10	Thiophosphorsäure-fluoralkylester
DE2709908A1 (de)	1978-09-14	Carbamoyloxysubstituierte pyrimidinyl(thiono)-(thiol)-phosphor(phosphon)-saeureester bzw. -esteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0535461A1 (de)	1993-04-07	Phosphorylierte Diazacycloalkane
EP0572440A1 (de)	1993-12-08	Substituierte pyridylpyrimidine, deren herstellung, ihre verwendung und neue zwischenprodukte.
EP0335212A2 (de)	1989-10-04	Thionophosphorsäureamidester
EP0305840A2 (de)	1989-03-08	Pyrimidinyl(thiono)(thiol)-phosphorsäureester
EP0070443A1 (de)	1983-01-26	Thionophosphonsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE4318110A1 (de)	1994-12-08	Phosphor(phosphon)säure-Derivate
DD248277A5 (de)	1987-08-05	Schaedlingsbekaempfungsmittel
DE3238363A1 (de)	1984-04-19	Thiophosphonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel