IL35041A - Esters of phosphonic acids, their production and pesticides containing them - Google Patents

Esters of phosphonic acids, their production and pesticides containing them

Info

Publication number: IL35041A
Authority: IL; Israel
Prior art keywords: phosphonic acid; acid ester; formula; same; methyl
Prior art date: 1969-08-11

Application number

IL35041A

Other languages

English (en)

Hebrew (he)

Other versions

IL35041A0 (en

Original Assignee

Ciba Geigy 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.)

1969-08-11

Filing date

1970-08-03

Publication date

1973-05-31

1970-08-03 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1970-10-30 Publication of IL35041A0 publication Critical patent/IL35041A0/xx

1973-05-31 Publication of IL35041A publication Critical patent/IL35041A/en

Links

150000003008 phosphonic acid esters Chemical class 0.000 title claims description 15
238000004519 manufacturing process Methods 0.000 title claims description 10
230000000361 pesticidal effect Effects 0.000 title claims description 8
239000000203 mixture Substances 0.000 title claims description 7
150000001875 compounds Chemical class 0.000 claims description 13
238000000034 method Methods 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 8
238000002360 preparation method Methods 0.000 claims description 8
239000002904 solvent Substances 0.000 claims description 7
241000238631 Hexapoda Species 0.000 claims description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
241000238876 Acari Species 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
239000002270 dispersing agent Substances 0.000 claims description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
239000011230 binding agent Substances 0.000 claims description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
125000001309 chloro group Chemical group Cl* 0.000 claims 3
239000004480 active ingredient Substances 0.000 claims 2
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
239000003085 diluting agent Substances 0.000 claims 1
239000012948 isocyanate Substances 0.000 claims 1
239000000575 pesticide Substances 0.000 claims 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
239000013543 active substance Substances 0.000 description 19
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
-1 lso Species 0.000 description 6
229910019142 PO4 Inorganic materials 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
239000008187 granular material Substances 0.000 description 5
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
239000010452 phosphate Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
238000005507 spraying Methods 0.000 description 5
239000000126 substance Substances 0.000 description 5
241000607479 Yersinia pestis Species 0.000 description 4
238000010410 dusting Methods 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 4
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 3
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
239000005977 Ethylene Substances 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
235000013311 vegetables Nutrition 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
241001674048 Phthiraptera Species 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
150000008065 acid anhydrides Chemical class 0.000 description 2
230000037396 body weight Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
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 2
238000002156 mixing Methods 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
229920002239 polyacrylonitrile Polymers 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
QAQSNXHKHKONNS-UHFFFAOYSA-N 1-ethyl-2-hydroxy-4-methyl-6-oxopyridine-3-carboxamide Chemical compound CCN1C(O)=C(C(N)=O)C(C)=CC1=O QAQSNXHKHKONNS-UHFFFAOYSA-N 0.000 description 1
WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 1
TZPPDWDHNIMTDQ-UHFFFAOYSA-N 2-dimethoxyphosphorylethanol Chemical compound COP(=O)(OC)CCO TZPPDWDHNIMTDQ-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 1
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
241001580838 Acarapis woodi Species 0.000 description 1
241001136265 Agriotes Species 0.000 description 1
241000218473 Agrotis Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241001220430 Aphelenchus Species 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
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241000894006 Bacteria Species 0.000 description 1
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OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
229920000298 Cellophane Polymers 0.000 description 1
DBUCFOVFALNEOO-HWBIYQLFSA-N Cevadine Chemical compound C1[C@@H](C)CC[C@H]2[C@](O)(C)[C@@]3(O)[C@@H](O)C[C@@]4(O)[C@@H]5CC[C@H]6[C@]7(C)CC[C@H](OC(=O)C(\C)=C/C)[C@@]6(O)O[C@@]75C[C@@]4(O)[C@@H]3CN21 DBUCFOVFALNEOO-HWBIYQLFSA-N 0.000 description 1
241000426497 Chilo suppressalis Species 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
241001641895 Dermestes Species 0.000 description 1
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
241000255925 Diptera Species 0.000 description 1
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OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
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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 1
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HAGICMWSNRLARD-UHFFFAOYSA-N N1=CC=CC(=C1)C1N(C)CCC1.C1(CC1)C(=O)O Chemical compound N1=CC=CC(=C1)C1N(C)CCC1.C1(CC1)C(=O)O HAGICMWSNRLARD-UHFFFAOYSA-N 0.000 description 1
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NQKSCAOXRSORTR-UHFFFAOYSA-N OP(O)(O)=S.Cl Chemical compound OP(O)(O)=S.Cl NQKSCAOXRSORTR-UHFFFAOYSA-N 0.000 description 1
GOQNKRPYPIQLQG-UHFFFAOYSA-N OP(O)(O)=S.OP(O)(O)=S Chemical compound OP(O)(O)=S.OP(O)(O)=S GOQNKRPYPIQLQG-UHFFFAOYSA-N 0.000 description 1
YMGWFZKTJHQTLC-UHFFFAOYSA-N OP(O)(O)=S.OP(O)(S)=S Chemical compound OP(O)(O)=S.OP(O)(S)=S YMGWFZKTJHQTLC-UHFFFAOYSA-N 0.000 description 1
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ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
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QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
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XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
CPGKMLVTFNUAHL-UHFFFAOYSA-N [Ca].[Ca] Chemical compound [Ca].[Ca] CPGKMLVTFNUAHL-UHFFFAOYSA-N 0.000 description 1
VDCKPZSNGOLFIN-UHFFFAOYSA-N [chloro(phenyl)-lambda4-sulfanylidene]-trihydroxy-lambda5-phosphane Chemical compound C1=CC=C(C=C1)S(=P(O)(O)O)Cl VDCKPZSNGOLFIN-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
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229910000278 bentonite Inorganic materials 0.000 description 1
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125000005605 benzo group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000011575 calcium Substances 0.000 description 1
HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
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150000001735 carboxylic acids Chemical class 0.000 description 1
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239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
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WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
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OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
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QSAZNTFFELIFAJ-UHFFFAOYSA-N s-chloro carbamothioate Chemical compound NC(=O)SCl QSAZNTFFELIFAJ-UHFFFAOYSA-N 0.000 description 1
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CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
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239000008096 xylene Substances 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
- C07F9/28—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
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl

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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)
Agricultural Chemicals And Associated Chemicals (AREA)

IL35041A 1969-08-11 1970-08-03 Esters of phosphonic acids, their production and pesticides containing them IL35041A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1213069A CH514988A (de)	1969-08-11	1969-08-11	Schädlingsbekämpfungsmittel

Publications (2)

Publication Number	Publication Date
IL35041A0 IL35041A0 (en)	1970-10-30
IL35041A true IL35041A (en)	1973-05-31

Family

ID=4380153

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL35041A IL35041A (en)	1969-08-11	1970-08-03	Esters of phosphonic acids, their production and pesticides containing them

Country Status (8)

Country	Link
US (2)	US3705212A (de)
BE (1)	BE754644A (de)
CH (1)	CH514988A (de)
DE (1)	DE2038011A1 (de)
FR (1)	FR2056670A5 (de)
GB (1)	GB1317295A (de)
IL (1)	IL35041A (de)
NL (1)	NL7011790A (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2903592A1 (de)	1979-01-31	1980-08-14	Bayer Ag	Phosphorylierte carbamoylverbindungen, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
US7767234B2 (en) *	2006-03-31	2010-08-03	John I. Haas, Inc.	Compositions and methods for controlling a honey bee parasitic mite
AU2014203897A1 (en)	2013-01-07	2015-07-23	John I. Haas, Inc.	Compositions and methods for controlling a honey bee parasitic mite infestation
CA3043388A1 (en)	2018-05-14	2019-11-14	John I. Hass, Inc.	Compositions and methods for controlling a honey bee parasitic mite infestation

1969
- 1969-08-11 CH CH1213069A patent/CH514988A/de not_active IP Right Cessation
1970
- 1970-07-31 DE DE19702038011 patent/DE2038011A1/de active Pending
- 1970-08-03 IL IL35041A patent/IL35041A/en unknown
- 1970-08-06 FR FR7029032A patent/FR2056670A5/fr not_active Expired
- 1970-08-06 US US61819A patent/US3705212A/en not_active Expired - Lifetime
- 1970-08-10 NL NL7011790A patent/NL7011790A/xx unknown
- 1970-08-10 BE BE754644D patent/BE754644A/xx unknown
- 1970-08-11 GB GB3865170A patent/GB1317295A/en not_active Expired
1972
- 1972-11-14 US US00306502A patent/US3781425A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
US3705212A (en)	1972-12-05
FR2056670A5 (de)	1971-05-14
CH514988A (de)	1971-11-15
GB1317295A (en)	1973-05-16
NL7011790A (de)	1971-02-15
IL35041A0 (en)	1970-10-30
BE754644A (fr)	1971-02-10
DE2038011A1 (de)	1971-03-04
US3781425A (en)	1973-12-25

Publication	Publication Date	Title
US4081536A (en)	1978-03-28	N-[(phosphinyl) amino]thio- and N-[(phosphinothioyl)amino]-thio-methylcarbamates and methods for controlling insects
IL35041A (en)	1973-05-31	Esters of phosphonic acids, their production and pesticides containing them
US3421883A (en)	1969-01-14	Pesticidal preparation and method of use
US4024277A (en)	1977-05-17	Phosphoro-aminosulfenyl derivatives of benzofuran carbamates
US3321516A (en)	1967-05-23	Dialkylthiocarbamylphosphonic diamides
US3732343A (en)	1973-05-08	1-halo-2-aryloxy-vinyl (2)-phosphates
US3551529A (en)	1970-12-29	Di-lower alkyl phosphites of 2-(lower-alkylthio)alkanaldoximes
US4115582A (en)	1978-09-19	N-1,1,2,2-tetrachloro-2-fluoroethylthio benzanilide and its use as fungicide and acaricide
US2995486A (en)	1961-08-08	Method for combating pests and preparations suitable therefor
US3644598A (en)	1972-02-22	1 - alkoxy(-alkenyloxy -phenoxy) - 1-thiono-3-chloro(3-alkyl)phospholines
US3267181A (en)	1966-08-16	Phosphorodithioates
US4203979A (en)	1980-05-20	Insecticidal 1-sec. and tert.-alkyl-2-disubstituted-phosphoryl hydrazines
IL32639A (en)	1972-10-29	Heterocyclic esters of thio- or diethio-phosphoric acid, their preparation and use as pesticides
US3432599A (en)	1969-03-11	Organophosphorus insecticides
US3852438A (en)	1974-12-03	Pesticidal compositions containing 1-halo-2-aryloxy-vinyl-(2)-phosphates
US3472933A (en)	1969-10-14	Pesticidal preparations containing carbonyl and thiocarbonyl phosphates and method of employing the same
US3840660A (en)	1974-10-08	Control of plant pathogenic fungi with 1-halo-2-aryloxy-vinyl-(2)phosphates
US3530206A (en)	1970-09-22	O,o-diloweralkyl-o - (2-chloro - 4 - bromo phenyl) phosphates and thiophosphates
CA1050567A (en)	1979-03-13	Formamidines
EP0031689B1 (de)	1983-09-28	O-aryl-S-tertiär-alkyl-alkylphosphonsäuredithioate-Insektizide und -Nematozide
US3641222A (en)	1972-02-08	S.s-dialkyl-amido-dithiophosphates
US3755506A (en)	1973-08-28	Phosphoryl cyanodithioimido carbonates
US3755571A (en)	1973-08-28	Use of substituted 1,2,4-thiadiazoles for killing insects
IL40476A (en)	1976-02-29	O,s-dialkyl-o-phenyl thiophosphoric acid esters,their manufacture and their use in pest control
US3264179A (en)	1966-08-02	Fungicidal phosphonamidothioates