CS233750B2 - Insecticide,acaricide and haematocide agent and processing of effective component - Google Patents

Insecticide,acaricide and haematocide agent and processing of effective component Download PDF

Info

Publication number: CS233750B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; alkyl; active ingredient; compounds; compound
Prior art date: 1982-07-31

Application number

CS835685A

Other languages

Czech (cs)

English (en)

Inventor

Gerhard Staehler

Werner Knauf

Burkhard Sachse

Anna Waltersdorfer

Original Assignee

Hoechst Ag

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.)

1982-07-31

Filing date

1983-07-29

Publication date

1985-03-14

1983-07-29 Application filed by Hoechst Ag filed Critical Hoechst Ag

1985-03-14 Publication of CS233750B2 publication Critical patent/CS233750B2/cs

Links

230000000895 acaricidal effect Effects 0.000 title claims description 5
239000000642 acaricide Substances 0.000 title claims 2
239000002917 insecticide Substances 0.000 title claims 2
239000003795 chemical substances by application Substances 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 40
229910052717 sulfur Inorganic materials 0.000 claims description 27
239000004480 active ingredient Substances 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 19
-1 alkali metal cation Chemical class 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
238000002360 preparation method Methods 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
239000002904 solvent Substances 0.000 claims description 5
238000009835 boiling Methods 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000003282 alkyl amino group Chemical group 0.000 claims description 3
125000004663 dialkyl amino group Chemical group 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
239000012442 inert solvent Substances 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
229910052783 alkali metal Inorganic materials 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
229910052757 nitrogen Inorganic materials 0.000 description 125
239000002253 acid Substances 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
230000000694 effects Effects 0.000 description 8
244000046052 Phaseolus vulgaris Species 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000008187 granular material Substances 0.000 description 5
241000196324 Embryophyta Species 0.000 description 4
241000244206 Nematoda Species 0.000 description 4
235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
235000008504 concentrate Nutrition 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
238000009472 formulation Methods 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
241000238876 Acari Species 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241001124076 Aphididae Species 0.000 description 3
241000233866 Fungi Species 0.000 description 3
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 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 3
239000013543 active substance Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
241000239290 Araneae Species 0.000 description 2
241001674044 Blattodea Species 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229920001214 Polysorbate 60 Polymers 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
240000006677 Vicia faba Species 0.000 description 2
235000010749 Vicia faba Nutrition 0.000 description 2
230000002745 absorbent Effects 0.000 description 2
239000002250 absorbent Substances 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
238000000227 grinding Methods 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
230000001418 larval effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000001069 nematicidal effect Effects 0.000 description 2
235000014483 powder concentrate Nutrition 0.000 description 2
239000011347 resin Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000000725 suspension Substances 0.000 description 2
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
OWFJMIVZYSDULZ-PXOLEDIWSA-N (4s,4ar,5s,5ar,6s,12ar)-4-(dimethylamino)-1,5,6,10,11,12a-hexahydroxy-6-methyl-3,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(=O)C(C(N)=O)=C(O)[C@@]4(O)C(=O)C3=C(O)C2=C1O OWFJMIVZYSDULZ-PXOLEDIWSA-N 0.000 description 1
241001672675 Adoxophyes Species 0.000 description 1
241000352333 Amegilla alpha Species 0.000 description 1
244000144730 Amygdalus persica Species 0.000 description 1
241000254177 Anthonomus Species 0.000 description 1
241001600407 Aphis <genus> Species 0.000 description 1
241001600408 Aphis gossypii Species 0.000 description 1
241000238659 Blatta Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241001157813 Cercospora Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000462639 Epilachna varivestis Species 0.000 description 1
241000221785 Erysiphales Species 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
235000009438 Gossypium Nutrition 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
241001201681 Hedya Species 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
241000287076 Monacha Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
241000721623 Myzus Species 0.000 description 1
241000488581 Panonychus citri Species 0.000 description 1
240000001090 Papaver somniferum Species 0.000 description 1
235000008753 Papaver somniferum Nutrition 0.000 description 1
241000219833 Phaseolus Species 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
241000233614 Phytophthora Species 0.000 description 1
241000233622 Phytophthora infestans Species 0.000 description 1
241001281803 Plasmopara viticola Species 0.000 description 1
241000242594 Platyhelminthes Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000006040 Prunus persica var persica Nutrition 0.000 description 1
241000918584 Pythium ultimum Species 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical compound OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
241001238452 Tortrix Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
240000006365 Vitis vinifera Species 0.000 description 1
235000014787 Vitis vinifera Nutrition 0.000 description 1
FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical compound CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
239000000701 coagulant Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000010411 cooking Methods 0.000 description 1
FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical compound O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000002996 emotional effect Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000003031 feeding effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
229910052622 kaolinite Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
125000001477 organic nitrogen group Chemical group 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000010998 test method Methods 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2408—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyalkyl compounds
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- 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
- 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- 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
- A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4075—Esters with hydroxyalkyl compounds

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS835685A 1982-07-31 1983-07-29 Insecticide,acaricide and haematocide agent and processing of effective component CS233750B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19823228631 DE3228631A1 (de)	1982-07-31	1982-07-31	Neue (di)-thiophosphor- und phosphonsaeure-derivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung im pflanzenschutz

Publications (1)

Publication Number	Publication Date
CS233750B2 true CS233750B2 (en)	1985-03-14

Family

ID=6169795

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS835685A CS233750B2 (en)	1982-07-31	1983-07-29	Insecticide,acaricide and haematocide agent and processing of effective component

Country Status (17)

Country	Link
US (1)	US4564611A (pt)
EP (1)	EP0100528A3 (pt)
JP (1)	JPS5944394A (pt)
KR (1)	KR840005458A (pt)
AU (1)	AU1745483A (pt)
BR (1)	BR8304072A (pt)
CS (1)	CS233750B2 (pt)
DD (1)	DD212889A5 (pt)
DE (1)	DE3228631A1 (pt)
DK (1)	DK349683A (pt)
ES (1)	ES524582A0 (pt)
GR (1)	GR79351B (pt)
IL (1)	IL69373A0 (pt)
OA (1)	OA07513A (pt)
PH (1)	PH18654A (pt)
TR (1)	TR22033A (pt)
ZA (1)	ZA835560B (pt)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5117057A (en) *	1985-10-21	1992-05-26	Rohm And Haas Company	Insecticidal N' substituted-N-N'-disubstituted-hydrazines
US4985461A (en) *	1985-10-21	1991-01-15	Rohm And Haas Company	Insecticidal N'-substituted-N,N'-diacylhydrazines
US5354762A (en) *	1986-07-14	1994-10-11	Rohm And Haas Company	Six-membered heterocyclic derivatives of N'-substituted N,N'-diacylhydrazines
US5424333A (en) *	1985-10-21	1995-06-13	Rohm And Haas Company	Anthelmintic N'-substituted-N,N'-disubstitutedhydrazines
DK483586A (da) *	1985-10-21	1987-04-22	Rohm & Haas	Insecticide n'-substituerede-n,n'-diacylhydraziner
CA1338289C (en) *	1986-01-22	1996-04-30	Raymond August Murphy	Insecticidal n'-substituted-n-alkylcarbonyl- n'-acylhydrazines
CA1295618C (en) *	1986-02-28	1992-02-11	Adam Chi-Tung Hsu	Insecticidal n'-substituted-n-acyl -n'-alkylcarbonylhydrazines
US5225443A (en) *	1986-05-01	1993-07-06	Rohm And Haas Company	Insecticidal N'-substituted-N'-substituted N,N'-diacylhydrazines
ATE61044T1 (de) *	1987-04-15	1991-03-15	Rohm & Haas	Insektizide n-(gegebenenfalls substituierte)-n'substituierte-n,n'-disubstituierte hydrazine.
US6013836A (en) *	1992-02-28	2000-01-11	Rohm And Haas Company	Insecticidal N'-substituted-N,N'-disubstitutedhydrazines

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3518327A (en) *	1967-04-10	1970-06-30	Stauffer Chemical Co	Phosphoro and phosphono acetylhydrazides
DE1920503A1 (de) *	1969-04-23	1970-11-05	Bayer Ag	O-Alkyl-N-monoalkylamido-(thiono)-thiolphosphorsaeure-S-(N,N-dialkylamino-carbamyl)-methylester und Verfahren zu ihrer Herstellung
US3678165A (en) *	1970-03-19	1972-07-18	Stauffer Chemical Co	Pesticidal phosphoro and phosphono acetylhydrazides
FR2123205A1 (en) *	1971-01-29	1972-09-08	Roussel Uclaf	Phosphorylthio acetohydrazides - having acaricidal activity

1982
- 1982-07-31 DE DE19823228631 patent/DE3228631A1/de not_active Withdrawn
1983
- 1983-07-27 TR TR22033A patent/TR22033A/xx unknown
- 1983-07-28 US US06/518,295 patent/US4564611A/en not_active Expired - Fee Related
- 1983-07-28 EP EP83107429A patent/EP0100528A3/de not_active Withdrawn
- 1983-07-29 BR BR8304072A patent/BR8304072A/pt unknown
- 1983-07-29 OA OA58080A patent/OA07513A/xx unknown
- 1983-07-29 CS CS835685A patent/CS233750B2/cs unknown
- 1983-07-29 JP JP58137914A patent/JPS5944394A/ja active Pending
- 1983-07-29 PH PH29311A patent/PH18654A/en unknown
- 1983-07-29 ZA ZA835560A patent/ZA835560B/xx unknown
- 1983-07-29 AU AU17454/83A patent/AU1745483A/en not_active Abandoned
- 1983-07-29 IL IL69373A patent/IL69373A0/xx unknown
- 1983-07-29 KR KR1019830003533A patent/KR840005458A/ko not_active Application Discontinuation
- 1983-07-29 ES ES524582A patent/ES524582A0/es active Granted
- 1983-07-29 DK DK349683A patent/DK349683A/da unknown
- 1983-07-29 DD DD83253535A patent/DD212889A5/de unknown
- 1983-07-29 GR GR72094A patent/GR79351B/el unknown

Also Published As

Publication number	Publication date
EP0100528A2 (de)	1984-02-15
OA07513A (fr)	1985-03-31
US4564611A (en)	1986-01-14
KR840005458A (ko)	1984-11-12
DK349683D0 (da)	1983-07-29
ES8404151A1 (es)	1984-05-01
JPS5944394A (ja)	1984-03-12
DE3228631A1 (de)	1984-02-02
ZA835560B (en)	1984-03-28
IL69373A0 (en)	1983-11-30
TR22033A (tr)	1986-07-03
ES524582A0 (es)	1984-05-01
BR8304072A (pt)	1984-03-07
DK349683A (da)	1984-02-01
EP0100528A3 (de)	1984-08-01
DD212889A5 (de)	1984-08-29
PH18654A (en)	1985-08-23
GR79351B (pt)	1984-10-22
AU1745483A (en)	1984-02-02

Publication	Publication Date	Title
CA1105930A (en)	1981-07-28	Insecticidal 2-substituted-imino-3-alkyl-5- dialkoxyphosphinothioyloxy-6h-1,3,4-thiadiazine
CS233750B2 (en)	1985-03-14	Insecticide,acaricide and haematocide agent and processing of effective component
US4152428A (en)	1979-05-01	Pesticidal agents
CA1048047A (en)	1979-02-06	Esters
IL45780A (en)	1977-12-30	Urea thiolphosphonates their preparation and their use in pest control
US4172080A (en)	1979-10-23	Phosphorus esters of 1-cyanoethyl-1,2,4-triazol-3-ols
EP0065216A1 (de)	1982-11-24	Pestizide S-(1.2.4-Triazol-5-ylmethyl)-(di)-thiophosph(on)ate und Verfahren zu ihrer Herstellung
US3676555A (en)	1972-07-11	Insecticidal and acaricidal amido-thiolphosphoric acid esters
CA1042461A (en)	1978-11-14	Pesticidal 1,3,5-triazapenta-1,4-dienes
US3760043A (en)	1973-09-18	O-phenyl-s-alkyl-n-alkyl-phosphoroamido-thiolates
US4140795A (en)	1979-02-20	Pesticidal 1,3,5-triazapenta-1,4-dienes
US3968222A (en)	1976-07-06	Insecticidal O,S-dialkyl esters of pyridylthio-and-pyridyldithio-phosphoric acids
GB1579592A (en)	1980-11-19	Cyclopropylmethylthio phosphoric acid derivatives
US4439430A (en)	1984-03-27	O,O-Diethyl O-[(p-tertiarybutylthio)phenyl]phosphorothioates and its insecticidal use
US3920671A (en)	1975-11-18	Certain phosphorus acid esters
IL43144A (en)	1977-02-28	Thiophosphoric acid amide esters their preparation and their use in insecticidal acaricidal and nematicidal compositions
US4599329A (en)	1986-07-08	O,S-dialkyl S-[carbamyloxyalkyl] dithiophosphates and their use as pesticides
EP0068823B1 (en)	1988-05-04	Novel phosphoro (di or tri) thioate derivatives, pesticidal compositions containing them and the use of the novel derivatives for combating pests
US3919129A (en)	1975-11-11	Certain phosphorus acid esters
US4556650A (en)	1985-12-03	Phosphonic acid esters as pesticides
US4581350A (en)	1986-04-08	O-(perfluoroalkylthiophenyl) (thio or amido) phosphates as pesticides
CA1037049A (en)	1978-08-22	Succinic acid oximidophosphoric esters
US4042691A (en)	1977-08-16	Succinic acid oximidophosphoric ester insecticides
IL36583A (en)	1973-11-28	Thiophosphoric acid esters and their use as pesticides
IL29992A (en)	1972-07-26	Novel phosphorothiolates