SU1743175A1 - Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity - Google Patents

Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity

Info

Publication number
SU1743175A1
SU1743175A1 SU4860403/04A SU4860403A SU1743175A1 SU 1743175 A1 SU1743175 A1 SU 1743175A1 SU 4860403/04 A SU4860403/04 A SU 4860403/04A SU 4860403 A SU4860403 A SU 4860403A SU 1743175 A1 SU1743175 A1 SU 1743175A1
Authority
SU
USSR - Soviet Union
Prior art keywords
phenoxyphenoxy
ethyl
diamides
thiophosphoric acid
chnops
Prior art date
Application number
SU4860403/04A
Other languages
Russian (ru)
Inventor
А.Ф. Грапов
Л.В. Разводовская
Е.А. Чертополохова
Г.Б. Иванова
И.В. Климова
Original Assignee
Всесоюзный научно-исследовательский институт химических средств защиты растений
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.)
Filing date
Publication date
Application filed by Всесоюзный научно-исследовательский институт химических средств защиты растений filed Critical Всесоюзный научно-исследовательский институт химических средств защиты растений
Priority to SU4860403/04A priority Critical patent/SU1743175A1/en
Application granted granted Critical
Publication of SU1743175A1 publication Critical patent/SU1743175A1/en

Links

Abstract

FIELD: organic chemistry. SUBSTANCE: product: O-[2-(4-phenoxyphenoxy)ethyl] -N, N′-dimethyldiamidothiophosph- ate, empirical formula is CHNOPS, yield is 77% , m. p. is 52.5-53 C; O-[2-(4-phenoxyphenoxy)ethyl] -N, N′-diethyldiamidothiophospha- te, empirical formula is CHNOPS, yield is 51%, m. p. is 59-60 C; O-[2-(4-phenoxyphenoxy)ethyl] -N, N′-dipropyldiamidothiophosph- ate, empirical formula is CHNOPS, yield is 56$, nD= 1.5610. Reagent 1: dichloroanhydride of O-[2-(4-phenoxyphenoxy)ethylthiophosphoric acid. Reagent 2: alkylamine. Reaction conditions: in the medium of organic solvent. Synthesized compounds are used in agriculture. EFFECT: improved method of synthesis. 2 tbl
SU4860403/04A 1990-08-17 1990-08-17 Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity SU1743175A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU4860403/04A SU1743175A1 (en) 1990-08-17 1990-08-17 Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU4860403/04A SU1743175A1 (en) 1990-08-17 1990-08-17 Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity

Publications (1)

Publication Number Publication Date
SU1743175A1 true SU1743175A1 (en) 1994-12-30

Family

ID=60521709

Family Applications (1)

Application Number Title Priority Date Filing Date
SU4860403/04A SU1743175A1 (en) 1990-08-17 1990-08-17 Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity

Country Status (1)

Country Link
SU (1) SU1743175A1 (en)

Similar Documents

Publication Publication Date Title
Kunz et al. The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐Glycopeptides
US3502720A (en) N-(2-methyl-4-chlorophenyl)-formamidines
SU1743175A1 (en) Diamides of o-[2-(4-phenoxyphenoxy)ethyl]thiophosphoric acid showing juvenile activity
JPS57116038A (en) Preparation of 3-cyano-3,5,5-trimethylcyclohexanone
SU1825496A3 (en) Derivatives of n-[4-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)phenyl- ]urea showing antidote activity to 2-chloro-n-[(4-methoxy-6-methyl-1,3,5-triazine-2-yl)aminocarb- onyl]benzene sulfamide in flax sowing
DE3061787D1 (en) Process for preparing derivatives of 6-amino-6-desoxy-2,3-0-isopropylidene-alpha-l-sorbofuranose and intermediates of the process
Reddy et al. A Novel, Simple and Rapid Protocol For N-Protected-oxazolidine-5-ones
EP0271443A1 (en) N,N'-disubstituted ureas and process for their production
ES2073370A1 (en) Process for the preparation of l-5-(2- - acetoxy-propionylamino)-2,4,6-triiodoisophthalic acid bis-(1,3-dihydroxy-propylamide)
SU1732666A1 (en) Thiophosphorylated lactam oximes showing insecto-acaricidic activity
SU1783780A1 (en) N-[((2,5-dimethylphenyl)sulfonyl)-aminocarbonyl]-amide of phenoxyacetic acid showing growth-regulating activity
ATE14118T1 (en) PROCESS FOR PREPARING N-METHOXY-N-METHYL-URETHANES.
JPS62249996A (en) Novel benzoxazaphosphorine derivative and insecticidal composition containing said derivative as active ingredient
SU1743158A1 (en) 1-glycidylimidazoles as cohardening agents of epoxy resins
JPS6483031A (en) Synthesis of fluorohydrin
RU95104673A (en) Pyridine schiff's base as vulcanizing agent in rubber mixture and method of their synthesis
SU1809602A1 (en) 3-phenoxybenzylaminoacetonitriles showing growth-regulating activity
SU1771186A1 (en) Para-chlorophenoxyacetic acid adamant-2-ylaminoethyl ester hydrochloride showing thermoprotective and psychostimulating activities
US3392167A (en) Novel s-tetrazine and method for preparing same
JPS5758645A (en) Preparation of carbonate
SU1334658A1 (en) Method of synthesis of m-chlorodiphenylmethylurea
US5066813A (en) Method for production of 1,3-thiazolidin-2-ones
Besenyei et al. Synthesis of arylsulfonylcarbamic acid derivatives using a new, phosgene-free method
SU1293981A1 (en) Method of synthesis of 2-amino-1,3,5-triazine derivatives
SU1780295A1 (en) Trans-2-n,n-dimethylaminopinocamphone oxime or its hydrochloride showing antifidant activity with relation to gnawing and suctional insects