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Chlorophosphoric acid-(2-chloro-ethyl ester)-phenyl ester, also known as phenyl chlorophosphonate or 2-chloroethyl phenyl chlorophosphonate, is a chemical compound with the molecular formula C8H8Cl2O2P. It is an organophosphorus compound that is formed by the esterification of chlorophosphoric acid with 2-chloroethanol and phenol. chlorophosphoric acid-(2-chloro-ethyl ester)-phenyl ester is characterized by its potential reactivity and is used in various chemical synthesis processes, particularly in the production of pesticides and other agrochemicals. Due to its reactivity and potential toxicity, it is important to handle chlorophosphoric acid-(2-chloro-ethyl ester)-phenyl ester with care, following appropriate safety protocols.

6719-83-1

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6719-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6719-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6719-83:
(6*6)+(5*7)+(4*1)+(3*9)+(2*8)+(1*3)=121
121 % 10 = 1
So 6719-83-1 is a valid CAS Registry Number.

6719-83-1Relevant academic research and scientific papers

Synthesis and fungicidal activity of O-alkyl O-aryl O-2-(stearamido)ethyl phosphates

Han, Liang,Gao, Jian-Rong,Li, Zheng-Ming

, p. 602 - 608 (2008/12/22)

N-stearoylethanolamine (NAE18:0) was reacted with O-alkyl O-aryl chlorophosphate and a series of O-alkyl O-aryl O-2-(stearamido)ethyl phosphates were synthesized to explore their antifungal activity. Compared with parent NAE18:0, title compounds without substitution or with methyl substitution on a benzene ring exhibited improved antifungal activity.

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