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Chloridothiophosphoric acid O-ethyl S-propyl ester, also known as O-ethyl S-propyl chloridothiophosphate, is an organophosphorus compound with the chemical formula C5H12ClO2PS. It is a colorless liquid with a pungent odor and is used as an intermediate in the synthesis of various pesticides, particularly organophosphorus insecticides. Chloridothiophosphoric acid O-ethyl S-propyl ester is highly toxic and can pose serious health risks if not handled properly, as it can cause respiratory, neurological, and gastrointestinal issues. Due to its potential hazards, it is crucial to follow safety guidelines and regulations when working with chloridothiophosphoric acid O-ethyl S-propyl ester.

7651-98-1

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7651-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7651-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7651-98:
(6*7)+(5*6)+(4*5)+(3*1)+(2*9)+(1*8)=121
121 % 10 = 1
So 7651-98-1 is a valid CAS Registry Number.

7651-98-1SDS

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 1-[chloro(ethoxy)phosphoryl]sulfanylpropane

1.2 Other means of identification

Product number -
Other names O-ethyl S-propyl phosphorochloridothioate

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:7651-98-1 SDS

7651-98-1Relevant academic research and scientific papers

The chlorination reaction of O-alkyl S-alkyl(aryl) thiophosphoric(-nic) acid derivatives with phosphorus oxychloride

He, Zheng-Jie,Chen, Wen-Bing,Ma, Fu-Peng,Zhou, Zheng-Hong,Tang, Chu-Chi

, p. 49 - 55 (2007/10/03)

It is reported that a variety of O-alkyl S-alkyl(aryl) thiophosphoric(-nic) acid derivatives 4 can be readily chlorinated with phosphorus oxychloride giving S-alkyl(aryl) thiophosphoro(-no)chloridates 2 and O-alkyl phosphorodichloridates 3.

Production of phosphoro chloride thiolates

-

, (2008/06/13)

A process for the production of a phosphoro chloride thiolate of the formula STR1 wherein R1 is alkyl, alkoxyalkyl, aryl, or aryl substituted by alkyl, alkoxy or halogen, and R2 is alkyl, comprising reacting a mixture of a dialkyl chlorophosphite of the formula and an alkyl dichloro-phosphite of the formula with a sulphenyl chloride of the formula to produce a mixture of a phosphorochloridothiolate of the formula STR2 and a phosphorodichloridothiolate of the formula STR3 and reacting the mixture without isolation with an alcohol of the formula in the presence of a dehydrochlorinating agent thereby to convert the phosphorodichloridothiolate of the formula STR4 to additional phosphorochloridothiolate STR5 The starting mixture is produced by reacting phosphorus trichloride with a trialkyl phosphite, or with an alcohol in the presence of a dehydrochlorinating agent.

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