IL34038A - Esters and ester-amides of phosphoric,thionophosphoric,phosphonic and thionophosphonic acids,their preparation and their use as insecticides and acaricides - Google Patents

Esters and ester-amides of phosphoric,thionophosphoric,phosphonic and thionophosphonic acids,their preparation and their use as insecticides and acaricides

Info

Publication number: IL34038A
Authority: IL; Israel
Prior art keywords: compound; formula; carbon atoms; process according; active
Prior art date: 1969-04-05

Application number

IL34038A

Other languages

English (en)

Other versions

IL34038A0 (en

Original Assignee

Bayer 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.)

1969-04-05

Filing date

1970-03-10

Publication date

1972-12-29

1970-03-10 Application filed by Bayer Ag filed Critical Bayer Ag

1970-05-21 Publication of IL34038A0 publication Critical patent/IL34038A0/xx

1972-12-29 Publication of IL34038A publication Critical patent/IL34038A/en

Links

239000002253 acid Substances 0.000 title claims description 10
150000002148 esters Chemical class 0.000 title claims description 7
230000000895 acaricidal effect Effects 0.000 title claims description 5
238000002360 preparation method Methods 0.000 title description 6
239000000642 acaricide Substances 0.000 title description 2
150000007513 acids Chemical class 0.000 title description 2
239000002917 insecticide Substances 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 47
239000000203 mixture Substances 0.000 claims description 16
238000000034 method Methods 0.000 claims description 12
239000002904 solvent Substances 0.000 claims description 12
239000003085 diluting agent Substances 0.000 claims description 11
-1 ester amides Chemical class 0.000 claims description 11
241000238631 Hexapoda Species 0.000 claims description 8
238000006243 chemical reaction Methods 0.000 claims description 7
230000006378 damage Effects 0.000 claims description 7
239000007788 liquid Substances 0.000 claims description 7
239000007787 solid Substances 0.000 claims description 7
239000004480 active ingredient Substances 0.000 claims description 4
230000000749 insecticidal effect Effects 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims 6
125000004432 carbon atom Chemical group C* 0.000 claims 6
125000003545 alkoxy group Chemical group 0.000 claims 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
229910052760 oxygen Inorganic materials 0.000 claims 2
239000001301 oxygen Substances 0.000 claims 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
239000005864 Sulphur Substances 0.000 claims 1
125000003118 aryl group Chemical group 0.000 claims 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
229910052794 bromium Inorganic materials 0.000 claims 1
229910052801 chlorine Inorganic materials 0.000 claims 1
239000000460 chlorine Substances 0.000 claims 1
125000004663 dialkyl amino group Chemical group 0.000 claims 1
229910052736 halogen Inorganic materials 0.000 claims 1
150000002367 halogens Chemical class 0.000 claims 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
229910052708 sodium Inorganic materials 0.000 claims 1
239000011734 sodium Substances 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 37
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
241000255925 Diptera Species 0.000 description 7
241000238876 Acari Species 0.000 description 6
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
241001454295 Tetranychidae Species 0.000 description 6
241000607479 Yersinia pestis Species 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
241001454293 Tetranychus urticae Species 0.000 description 5
239000000047 product Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
241000254173 Coleoptera Species 0.000 description 4
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
238000009472 formulation Methods 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
239000000243 solution Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
241001124076 Aphididae Species 0.000 description 3
241001510109 Blaberus giganteus Species 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
241000257159 Musca domestica Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
241000500437 Plutella xylostella Species 0.000 description 3
241000254179 Sitophilus granarius Species 0.000 description 3
241000254154 Sitophilus zeamais Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
239000000969 carrier Substances 0.000 description 3
XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
241000256118 Aedes aegypti Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
241000387321 Aspidiotus nerii Species 0.000 description 2
241000238657 Blattella germanica Species 0.000 description 2
241001674044 Blattodea Species 0.000 description 2
240000007124 Brassica oleracea Species 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
241001664260 Byturus tomentosus Species 0.000 description 2
241000257163 Calliphora vicina Species 0.000 description 2
241000255579 Ceratitis capitata Species 0.000 description 2
241001327638 Cimex lectularius Species 0.000 description 2
241000256059 Culex pipiens Species 0.000 description 2
241000255601 Drosophila melanogaster Species 0.000 description 2
241001581006 Dysaphis plantaginea Species 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
241000483001 Euproctis chrysorrhoea Species 0.000 description 2
239000004606 Fillers/Extenders Substances 0.000 description 2
241000255896 Galleria mellonella Species 0.000 description 2
241000257303 Hymenoptera Species 0.000 description 2
241000258916 Leptinotarsa decemlineata Species 0.000 description 2
241000255685 Malacosoma neustria Species 0.000 description 2
241000721623 Myzus Species 0.000 description 2
241000810465 Myzus cerasi cerasi Species 0.000 description 2
241000721621 Myzus persicae Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241001491877 Operophtera brumata Species 0.000 description 2
241000238814 Orthoptera Species 0.000 description 2
241000131101 Oryzaephilus surinamensis Species 0.000 description 2
241000238675 Periplaneta americana Species 0.000 description 2
241001396980 Phytonemus pallidus Species 0.000 description 2
241000255969 Pieris brassicae Species 0.000 description 2
241000952063 Polyphagotarsonemus latus Species 0.000 description 2
241000722238 Pseudococcus maritimus Species 0.000 description 2
241001509967 Reticulitermes flavipes Species 0.000 description 2
241000125167 Rhopalosiphum padi Species 0.000 description 2
235000001537 Ribes X gardonianum Nutrition 0.000 description 2
235000001535 Ribes X utile Nutrition 0.000 description 2
235000016919 Ribes petraeum Nutrition 0.000 description 2
244000281247 Ribes rubrum Species 0.000 description 2
235000002355 Ribes spicatum Nutrition 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
241000256251 Spodoptera frugiperda Species 0.000 description 2
241001177161 Stegobium paniceum Species 0.000 description 2
241001494115 Stomoxys calcitrans Species 0.000 description 2
241000254109 Tenebrio molitor Species 0.000 description 2
241001414989 Thysanoptera Species 0.000 description 2
241001238451 Tortrix viridana Species 0.000 description 2
241000267822 Trogoderma granarium Species 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000003513 alkali Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
239000004927 clay Substances 0.000 description 2
238000010410 dusting Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
229940052303 ethers for general anesthesia Drugs 0.000 description 2
239000008187 granular material Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000006072 paste Substances 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000002689 soil Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
241001143308 Acanthoscelides Species 0.000 description 1
241001143309 Acanthoscelides obtectus Species 0.000 description 1
241000238818 Acheta domesticus Species 0.000 description 1
241000253994 Acyrthosiphon pisum Species 0.000 description 1
241000426834 Aegina Species 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
241001136249 Agriotes lineatus Species 0.000 description 1
241000218475 Agrotis segetum Species 0.000 description 1
241000449794 Alabama argillacea Species 0.000 description 1
241001414900 Anopheles stephensi Species 0.000 description 1
241000238788 Blaberus craniifer Species 0.000 description 1
241000238659 Blatta Species 0.000 description 1
241000238662 Blatta orientalis Species 0.000 description 1
241000256593 Brachycaudus schwartzi Species 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000011303 Brassica alboglabra Nutrition 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
235000011302 Brassica oleracea Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
241000907225 Bruchidius Species 0.000 description 1
241001221118 Cecidophyopsis ribis Species 0.000 description 1
241000255930 Chironomidae Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
241000254137 Cicadidae Species 0.000 description 1
241001415288 Coccidae Species 0.000 description 1
241001465977 Coccoidea Species 0.000 description 1
241001479447 Coccus hesperidum Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241001094913 Cryptomyzus Species 0.000 description 1
241000289763 Dasygaster padockina Species 0.000 description 1
241001641895 Dermestes Species 0.000 description 1
241001513837 Dermestes maculatus Species 0.000 description 1
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
241001425477 Dysdercus Species 0.000 description 1
241000122098 Ephestia kuehniella Species 0.000 description 1
241000239245 Euscelis Species 0.000 description 1
241000233866 Fungi Species 0.000 description 1
241001675057 Gastrophysa viridula Species 0.000 description 1
241000258937 Hemiptera Species 0.000 description 1
241000652697 Henschoutedenia flexivitta Species 0.000 description 1
241001659688 Hercinothrips femoralis Species 0.000 description 1
241001251958 Hyalopterus Species 0.000 description 1
241001251909 Hyalopterus pruni Species 0.000 description 1
241000256602 Isoptera Species 0.000 description 1
241000948337 Lasius niger Species 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
241000721703 Lymantria dispar Species 0.000 description 1
241000721714 Macrosiphum euphorbiae Species 0.000 description 1
241000555303 Mamestra brassicae Species 0.000 description 1
241000254071 Melolontha Species 0.000 description 1
241000254099 Melolontha melolontha Species 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
241000961933 Nephotettix virescens Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241001481099 Ornithodoros turicata Species 0.000 description 1
241001548358 Parapiesma quadratum Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241000257149 Phormia Species 0.000 description 1
241000257186 Phormia regina Species 0.000 description 1
241000690748 Piesma Species 0.000 description 1
235000005805 Prunus cerasus Nutrition 0.000 description 1
241001097374 Pselliopus cinctus Species 0.000 description 1
241001510241 Rhyparobia Species 0.000 description 1
241000985245 Spodoptera litura Species 0.000 description 1
241001414831 Triatoma infestans Species 0.000 description 1
241000254113 Tribolium castaneum Species 0.000 description 1
241001466337 Yponomeuta Species 0.000 description 1
241000064240 Yponomeuta padellus Species 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
229960004132 diethyl ether Drugs 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
201000004792 malaria Diseases 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
230000017066 negative regulation of growth Effects 0.000 description 1
239000003921 oil Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
239000003128 rodenticide Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
241000894007 species Species 0.000 description 1
239000000758 substrate Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002699 waste material Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2479—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1)
- C07F9/2491—Compounds containing the structure P(=X)n-N-acyl, P(=X)n-N-heteroatom, P(=X)n-N-CN (X = O, S, Se; n = 0, 1) containing the structure P(=X)n-N-N (X = O, S, Se; n = 0, 1)
- 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
- C07F9/650905—Six-membered rings having the nitrogen atoms in the positions 1 and 2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Crystallography & Structural Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL34038A 1969-04-05 1970-03-10 Esters and ester-amides of phosphoric,thionophosphoric,phosphonic and thionophosphonic acids,their preparation and their use as insecticides and acaricides IL34038A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19691917741 DE1917741B2 (de)	1969-04-05	1969-04-05	(thiono)phosphor(phosphon) -saeureester bzw. -esteramide, verfahren zu ihrer herstellung sowie ihre verwendung

Publications (2)

Publication Number	Publication Date
IL34038A0 IL34038A0 (en)	1970-05-21
IL34038A true IL34038A (en)	1972-12-29

Family

ID=5730560

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL34038A IL34038A (en)	1969-04-05	1970-03-10	Esters and ester-amides of phosphoric,thionophosphoric,phosphonic and thionophosphonic acids,their preparation and their use as insecticides and acaricides

Country Status (11)

Country	Link
US (1)	US3700687A (fr)
JP (1)	JPS4840745B1 (fr)
BE (1)	BE748483A (fr)
BR (1)	BR7018014D0 (fr)
CH (1)	CH533640A (fr)
DE (1)	DE1917741B2 (fr)
ES (1)	ES378248A1 (fr)
FR (1)	FR2042935A5 (fr)
GB (1)	GB1249595A (fr)
IL (1)	IL34038A (fr)
NL (1)	NL7004833A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2548183A1 (de) *	1975-10-28	1977-05-05	Bayer Ag	Diphosphorylierte pyrazole, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide
US6637150B1 (en) *	1999-10-13	2003-10-28	University Of Florida	Below ground non-edible foraging matrix configurations for arthropod control

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH300758A (de) *	1951-04-20	1954-08-15	Ag J R Geigy	Verfahren zur Herstellung eines Phosphorsäureesters.
CH300741A (de) *	1951-04-20	1954-08-15	Ag J R Geigy	Verfahren zur Herstellung eines Phosphorsäureesters.
BE510817A (fr) *	1951-04-20	1900-01-01
NL237242A (fr) *	1958-03-18	1900-01-01
NL126404C (fr) *	1959-03-28	1900-01-01

1969
- 1969-04-05 DE DE19691917741 patent/DE1917741B2/de active Pending
1970
- 1970-03-05 CH CH322370A patent/CH533640A/de not_active IP Right Cessation
- 1970-03-10 IL IL34038A patent/IL34038A/en unknown
- 1970-03-30 JP JP45026068A patent/JPS4840745B1/ja active Pending
- 1970-03-31 US US24397A patent/US3700687A/en not_active Expired - Lifetime
- 1970-04-03 FR FR7012225A patent/FR2042935A5/fr not_active Expired
- 1970-04-03 BE BE748483D patent/BE748483A/fr unknown
- 1970-04-03 NL NL7004833A patent/NL7004833A/xx unknown
- 1970-04-03 BR BR218014/70A patent/BR7018014D0/pt unknown
- 1970-04-04 ES ES378248A patent/ES378248A1/es not_active Expired
- 1970-04-06 GB GB06223/70A patent/GB1249595A/en not_active Expired

Also Published As

Publication number	Publication date
FR2042935A5 (fr)	1971-02-12
DE1917741B2 (de)	1976-12-02
DE1917741A1 (de)	1970-10-15
CH533640A (de)	1973-02-15
BR7018014D0 (pt)	1973-05-08
IL34038A0 (en)	1970-05-21
US3700687A (en)	1972-10-24
BE748483A (fr)	1970-10-05
GB1249595A (en)	1971-10-13
JPS4840745B1 (fr)	1973-12-03
ES378248A1 (es)	1972-05-16
NL7004833A (fr)	1970-10-07

Publication	Publication Date	Title
US3801679A (en)	1974-04-02	N-(dimethylaminomethylidene)thiol-(thiono)-phosphoric acid ester imides s
IL47958A (en)	1977-08-31	Pyrimidinylthionophosphonic acid esters process for their preparation and insecticidal acaricidal and nematicidal compositions containing them
US4104377A (en)	1978-08-01	Disubstituted-O-(1-fluoro-2-halogenoethyl)-phosphoric(phosphonic) acid esters, and method of combating insects
US3954755A (en)	1976-05-04	7-Bromoquinoxal-6-yl-(thiono)-(thiol)-phosphoric and (phosphonic) acid esters of ester-amides
US3884996A (en)	1975-05-20	O,O-dialkyl-1-cyanoalkyl-ketonoxime-thionophosphoric acid esters
IL34985A (en)	1972-11-28	Triazolothiazole esters of phosphoric, phosphonic and phosphonic acids and of the appropriate tionic acids, their preparation and use as insecticides and acaricides
US4001404A (en)	1977-01-04	N-dithiophosphoryl-carbamic acid esters
IL34950A (en)	1973-01-30	Esters of thiazolo-phosphoric and -phosphonic,thiazolo-thionophosphoric and -thionophosphonic acid,their preparation and use as insecticides and acaricides
US3544572A (en)	1970-12-01	Thionophosphonic acid esters
IL31318A (en)	1972-04-27	Phosphoric,phosphonic or thionophosphoric(-phosphonic)acid esters of pyridazinediol,their preparation and pest control compositions containing them
US3974171A (en)	1976-08-10	O-[3-methyl-1,3,4-triazole-(2,3,-b)-thiazol(6)yl]-(thiono)-phosphoric(phosphonic) acid esters
US3894020A (en)	1975-07-08	3,4,-Dihydro-4-oxo-quinazolin (3)-yl-(thiono)-phosphoric (phosphonic) acid esters
IL37223A (en)	1973-11-28	Esters of O-pyrazolo-pyrimidine- (thionic) - phosphorous and phosphonic acids, their preparation and use as insecticides and mites
US4000268A (en)	1976-12-28	N,N-dimethyl-N'-[O-phenyl-(thiono)-alkane-phosphonyl]-formamidines
US3706820A (en)	1972-12-19	S-alkylmercaptomethylthiophosphoric or phosphonic acid esters
IL34038A (en)	1972-12-29	Esters and ester-amides of phosphoric,thionophosphoric,phosphonic and thionophosphonic acids,their preparation and their use as insecticides and acaricides
US4002744A (en)	1977-01-11	O-Ethyl-O-iso-butyl-O-(2,2-dichlorovinyl)-thiono-phosphoric acid ester
US4233293A (en)	1980-11-11	Insecticidal and acaricidal O-alkyl-O-[1-(2-cyanoalkyl)-5-halo-1,2,4-triazol(3)yl]-(thiono)(thiol)-phosphoric(phosphonic) acid esters and ester-amides
US3966920A (en)	1976-06-29	O,S-Dialkyl-O-(2-cyanophenyl)-thionothiolphosphoric acid esters and insecticidal and acaricidal compositions and method
US3700686A (en)	1972-10-24	O-alkyl-o-pyrazolyl-phosphoric, phosphonic, thionophosphoric and thionophosphonic acid esters
US3950334A (en)	1976-04-13	O-Alkyl-S-alkyl-O-[6-alkyl- or 6-halo-pyridazin-(3)-yl]-(thiono)thiol-phosphoric acid esters
IL34101A (en)	1972-12-29	O-alkyl-s-(n,n-dialkylaminocarbamyl)-methyl-n-monoalkylamido-thiolphosphoric and thionothiolphosphoric acid esters,their preparation and use as insecticides and acaricides
US3966850A (en)	1976-06-29	O-ethyl-S-n-propyl-O-(2-bromo-4-cyanophenyl)-thionothiol-phosphoric acid ester
US3981994A (en)	1976-09-21	O-Alkyl-O-[1-phenyl-5-cyanoalkylmercapto-1,2,4-triazol(3)yl]-thionophosphoric(phosphonic) acid esters
US3952098A (en)	1976-04-20	Compositions and methods of combatting insects and acarids using pyrazolo-(thiono)-phosphoric(phosphonic) acid esters