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(CHLOROCARBONYLDIFLUOROMETHYL)PHOSPHONIC ACID DIETHYL ESTER, with the molecular formula C5H8ClF2O4P, is a chemical compound that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a phosphonic acid diethyl ester, characterized by a phosphorus atom bonded to two oxygen atoms and two ethyl groups, along with a chlorocarbonyl group and a difluoromethyl group. Due to its potential hazards, it is crucial to handle (CHLOROCARBONYLDIFLUOROMETHYL)PHOSPHONIC ACID DIETHYL ESTER with care.

97480-49-4

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97480-49-4 Usage

Uses

Used in Pharmaceutical Industry:
(CHLOROCARBONYLDIFLUOROMETHYL)PHOSPHONIC ACID DIETHYL ESTER is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, (CHLOROCARBONYLDIFLUOROMETHYL)PHOSPHONIC ACID DIETHYL ESTER is utilized as a precursor in the production of agrochemicals. Its role in the synthesis process helps create effective solutions for agricultural applications, such as pesticides and herbicides, to protect crops and enhance yield.

Check Digit Verification of cas no

The CAS Registry Mumber 97480-49-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97480-49:
(7*9)+(6*7)+(5*4)+(4*8)+(3*0)+(2*4)+(1*9)=174
174 % 10 = 4
So 97480-49-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H10ClF2O4P/c1-3-12-14(11,13-4-2)6(8,9)5(7)10/h3-4H2,1-2H3

97480-49-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (Diethoxyphosphoryl)difluoroacetic acid

1.2 Other means of identification

Product number -
Other names difluoro(diethoxyphosphinyl)acetyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:97480-49-4 SDS

97480-49-4Relevant academic research and scientific papers

The amination of difluoro(diethoxyphosphoryl)acetyl chloride: Facile synthetic route to novel amides containing difluoromethylenephosphonate moiety

Pajkert, Romana,Milewska, Magdalena,R?schenthaler, Gerd-Volker,Koroniak, Henryk

experimental part, p. 695 - 701 (2009/12/24)

A convenient route for the synthesis of novel amides containing at least one β-keto-α,α-difluoromethylenephosphonate group has been elaborated. The procedure requires simple stirring of an amine and difluoro(diethoxyphosphoryl)acetyl chloride in THF in th

Preparation of Difluorophosphonoacetic Acid and Its Derivatives

Burton, Donald J.,Sprague, Lee G.

, p. 1523 - 1527 (2007/10/02)

The preparation of ethyl difluoro(diethoxyphosphinyl)acetate (1) has been effected by the acylation of zinc bromide with ethyl chloroformate in the presence of a catalytic amount of cuprous bromide.Similarly prepared were ethyl difluoro(diethoxyphosphinyl)pyruvate (2) and N,N-diethyldifluoro(diethoxyphosphinyl)acetamide (3).Bromotrimethylsilane selectively reacted with 1 to yield ethyl difluoroacetate (9).The remaining ethyl carboxylic ester of 9 reacted with iodotrimethylsilane to produce trimethylsilyl difluoroacetate (10), which was subsequently hydrolyzed to yield difluorophosphonoacetic acid (8).The phosphonate 9 was gently chlorinated to yield ethyl difluoro(dichlorophosphinyl)acetate (11).

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