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79236-72-9

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79236-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79236-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79236-72:
(7*7)+(6*9)+(5*2)+(4*3)+(3*6)+(2*7)+(1*2)=159
159 % 10 = 9
So 79236-72-9 is a valid CAS Registry Number.

79236-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name O,S-Dimethyl methylphosphonothioate

1.2 Other means of identification

Product number -
Other names -

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:79236-72-9 SDS

79236-72-9Downstream Products

79236-72-9Relevant articles and documents

Detoxification of O, S-diethyl methyl phosphonothiolate (OSDEMP), a simulant of VX, by N, N-dichlorourethane as an effective decontaminating agent

Singh, Ravindra,Gutch,Acharya,Prabha

experimental part, p. 1504 - 1509 (2011/12/02)

N, N-Dichlorourethane has been synthesized and characterized by FT-IR, NMR. Efficiency of this compound as decontaminant has been evaluated by the reaction of O, S-diethyl methyl phosphonothiolate (OSDEMP), a simulant of VX at RT. The decontamination reaction has been monitored by gas chromatography (GC) and the products have been identified by GC-MS.

Stereochemictry of Alkaline Hydrolyses of 1,3,2-Oxazaphospholidine-2-thiones and Related Reactions

Hall, C. Richard,Inch, Thomas D.

, p. 2368 - 2373 (2007/10/02)

Essentially exclusive cleavage, with retention of configuration, of the endocyclic P-O bond occurs during basic hydrolysis of 2-alkoxy-1,3,2-oxazaphospholidine-2-thiones.In the 2-methyl analogues, P-O bond cleavage occurs with both inversion and retention

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