DE2139691A1 - Substituierte fluorphosphazene - Google Patents

Substituierte fluorphosphazene

Info

Publication number: DE2139691A1
Authority: DE; Germany
Prior art keywords: parts; weight; substituted; active ingredient; nhch
Prior art date: 1971-08-07
Legal status (The legal status 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 status listed.): Pending

Application number

DE19712139691

Other languages

German (de)

English (en)

Inventor

Heinrich Dr Adolphi

Wolfgang Dr Bewert

Volker Dr Kiener

Gerd Dr Wunsch

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

BASF SE

Original Assignee

BASF SE

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.)

1971-08-07

Filing date

1971-08-07

Publication date

1973-02-15

Priority to BE787272D priority Critical patent/BE787272A/xx

1971-08-07 Application filed by BASF SE filed Critical BASF SE

1971-08-07 Priority to DE19712139691 priority patent/DE2139691A1/de

1972-08-04 Priority to CH1160072A priority patent/CH529791A/de

1972-08-04 Priority to GB3649572A priority patent/GB1388430A/en

1972-08-07 Priority to FR7228458A priority patent/FR2149955A5/fr

1973-02-15 Publication of DE2139691A1 publication Critical patent/DE2139691A1/de

Status Pending legal-status Critical Current

Links

125000000217 alkyl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
GRPIQKZLNSCFTB-UHFFFAOYSA-N n-[bis(dimethylamino)-fluoroimino-$l^{5}-phosphanyl]-n-methylmethanamine Chemical class CN(C)P(=NF)(N(C)C)N(C)C GRPIQKZLNSCFTB-UHFFFAOYSA-N 0.000 claims description 3
239000000575 pesticide Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
239000004480 active ingredient Substances 0.000 description 13
150000001875 compounds Chemical class 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
239000000203 mixture Substances 0.000 description 9
239000013543 active substance Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000000243 solution Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
229910052698 phosphorus Inorganic materials 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
238000009835 boiling Methods 0.000 description 4
-1 cycloalkyl radical Chemical class 0.000 description 4
239000007788 liquid Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 3
239000004359 castor oil Substances 0.000 description 3
235000019438 castor oil Nutrition 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
239000002904 solvent Substances 0.000 description 3
241001124076 Aphididae Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
241000500437 Plutella xylostella Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000004069 aziridinyl group Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000012141 concentrate Substances 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
238000004821 distillation Methods 0.000 description 2
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
238000005160 1H NMR spectroscopy Methods 0.000 description 1
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
241000256118 Aedes aegypti Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
241001674044 Blattodea Species 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
241000256113 Culicidae Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
241000500439 Plutella Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000003368 amide group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 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
239000004927 clay Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000012043 crude product Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
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 1
125000000468 ketone group Chemical group 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
238000000034 method Methods 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
125000002757 morpholinyl group Chemical group 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
150000004767 nitrides Chemical class 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
125000000719 pyrrolidinyl group Chemical group 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
238000010626 work up procedure 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/65812—Cyclic phosphazenes [P=N-]n, n>=3
- C07F9/65814—Cyclic phosphazenes [P=N-]n, n>=3 n = 3 or 4

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)
Agricultural Chemicals And Associated Chemicals (AREA)

DE19712139691 1971-08-07 1971-08-07 Substituierte fluorphosphazene Pending DE2139691A1 (de)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
BE787272D BE787272A (fr)	1971-08-07		Derives de substitution de fluophosphazenes
DE19712139691 DE2139691A1 (de)	1971-08-07	1971-08-07	Substituierte fluorphosphazene
CH1160072A CH529791A (de)	1971-08-07	1972-08-04	Verfahren zur Bekämpfung von Schädlingen
GB3649572A GB1388430A (en)	1971-08-07	1972-08-04	Pesticidal substituted fluorophosphazenes
FR7228458A FR2149955A5 (2)	1971-08-07	1972-08-07

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19712139691 DE2139691A1 (de)	1971-08-07	1971-08-07	Substituierte fluorphosphazene

Publications (1)

Publication Number	Publication Date
DE2139691A1 true DE2139691A1 (de)	1973-02-15

Family

ID=5816140

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19712139691 Pending DE2139691A1 (de)	1971-08-07	1971-08-07	Substituierte fluorphosphazene

Country Status (5)

Country	Link
BE (1)	BE787272A (2)
CH (1)	CH529791A (2)
DE (1)	DE2139691A1 (2)
FR (1)	FR2149955A5 (2)
GB (1)	GB1388430A (2)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2013047342A1 (ja)	2011-09-26	2013-04-04	富士フイルム株式会社	非水二次電池用電解液及び二次電池
CN116178442A (zh) *	2021-11-29	2023-05-30	宁德国泰华荣新材料有限公司	一种(2,2,2-三氟乙氧基)五氟环三磷腈的制备方法

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US9406972B2 (en) *	2012-05-04	2016-08-02	Samsung Sdi Co., Ltd.	Flame retardant monosubstituted pentafluorocyclotriphosphazene electrolyte additive and electrolyte including the same and rechargeable lithium battery including the same
JP6182113B2 (ja) *	2013-10-11	2017-08-16	富士フイルム株式会社	アミノ置換ホスファゼン化合物の製造方法、非水二次電池用電解液の製造方法および非水二次電池の製造方法
WO2016052329A1 (ja) *	2014-09-29	2016-04-07	富士フイルム株式会社	アミノ置換ホスファゼン化合物の製造方法、非水二次電池用電解液の製造方法および非水二次電池の製造方法

0
- BE BE787272D patent/BE787272A/xx unknown
1971
- 1971-08-07 DE DE19712139691 patent/DE2139691A1/de active Pending
1972
- 1972-08-04 GB GB3649572A patent/GB1388430A/en not_active Expired
- 1972-08-04 CH CH1160072A patent/CH529791A/de not_active IP Right Cessation
- 1972-08-07 FR FR7228458A patent/FR2149955A5/fr not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO2013047342A1 (ja)	2011-09-26	2013-04-04	富士フイルム株式会社	非水二次電池用電解液及び二次電池
CN116178442A (zh) *	2021-11-29	2023-05-30	宁德国泰华荣新材料有限公司	一种(2,2,2-三氟乙氧基)五氟环三磷腈的制备方法

Also Published As

Publication number	Publication date
GB1388430A (en)	1975-03-26
FR2149955A5 (2)	1973-03-30
CH529791A (de)	1972-10-31
BE787272A (fr)	1973-02-07

Legal Events

Date	Code	Title	Description
1978-11-16	OHA	Expiration of time for request for examination

Publication	Publication Date	Title
DE2609280A1 (de)	1977-09-15	Schaedlingsbekaempfungsmittel
DE3602169A1 (de)	1987-07-23	Neue alkan- und alkoxyalkanderivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende insektizide und akarizide mittel
DE1238902B (de)	1967-04-20	Verfahren zur Herstellung von Phosphor-, Phosphon- bzw. Thionophosphor-, -phosphon-saeureestern
CH621684A5 (2)	1981-02-27
DE3604781A1 (de)	1987-08-27	Neue silane, verfahren zu ihrer herstellung und diese verbindungen enthaltende einsektizide mittel
DE2139691A1 (de)	1973-02-15	Substituierte fluorphosphazene
DE2426653B2 (de)	1981-07-02	Derivate des 2-Amino-1,3-thiazins
DE2001770C3 (de)	1978-11-16	Amidothionophosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
DE1542715A1 (de)	1969-11-27	Schaedlingsbekaempfungsmittel
DE1215711B (de)	1966-05-05	Verfahren zur Herstellung von Dialkylzinn-bis-phenolaten
DE1643608A1 (de)	1972-05-04	Verfahren zur Herstellung neuer Phosphorester,sowie als Ausgangsstoffe dienender neuer alpha-Halogencyclobutanone und Verwendung der neuen Phosphorester zur Bekaempfung von Schaedlingen
DE1300113B (de)	1969-07-31	Dithiophosphorsaeureester und Verfahren zu ihrer Herstellung
CH488405A (de)	1970-04-15	Schädlingsbekämpfungsmittel
DE1181978B (de)	1964-11-19	Mittel zur Bekaempfung von Arthropoden, Mollusken und Fischen
DE2249939A1 (de)	1974-04-18	Phosphorsaeureester
DE2246939A1 (de)	1973-04-05	Organozinn-substituierte sulfolene und sulfolane, verfahren zu ihrer herstellung und diese verbindungen enthaltende mittel zur bekaempfung von schaedlingen
DE1542853C3 (de)	1976-02-26	Substituierte p-Cyanophenylcarbamate und diese enthaltende Schädlingsbekämpfungsmittel
DE974569C (de)	1961-03-02	Schaedlingsbekaempfungsmittel
DE2154371A1 (de)	1973-05-10	Fungizid fuer den pflanzenschutz
DE1198360B (de)	1965-08-12	Verfahren zur Herstellung von o-Alkyl-S-(l-phenyl-2-alkoxycarbonyl-äthyl) - alkylthiophosphonaten
CH629082A5 (de)	1982-04-15	Schaedlingsbekaempfungsmittel enthaltend neue dispirocyclopropancarbonsaeureester als wirkstoffkomponente.
DE2136395A1 (de)	1973-02-01	Insektizide phosphorsaeureester
DE2163063A1 (de)	1973-06-20	Dialkylthionophosphorsaeureester
AT258959B (de)	1967-12-27	Verfahren zur Herstellung von neuen Phosphorsäureestern
DE1187848B (de)	1965-02-25	Insektizides und akarizides Mittel

DE2139691A1 - Substituierte fluorphosphazene - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (5)

Applications Claiming Priority (1)

Publications (1)

Family

ID=5816140

Family Applications (1)

Country Status (5)

Cited By (2)

Families Citing this family (3)

Cited By (2)

Also Published As

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Legal Events