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Benzene, 1-[[2-[(2,4-dinitrophenyl)sulfonyl]ethyl]thio]-2,4-dinitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105472-31-9

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105472-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105472-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105472-31:
(8*1)+(7*0)+(6*5)+(5*4)+(4*7)+(3*2)+(2*3)+(1*1)=99
99 % 10 = 9
So 105472-31-9 is a valid CAS Registry Number.

105472-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitrophenyl 2-(2,4-dinitriphenylthio)ethyl sulfone

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:105472-31-9 SDS

105472-31-9Downstream Products

105472-31-9Relevant academic research and scientific papers

Sulfinic Acids and Related Compounds. 18. Synthesis and Properties of Derivatives of 2-Mercaptoethanesulfinic Acid

Harmon, J. Patrick,Field, Lamar

, p. 5235 - 5240 (1986)

Use of thiirane 1,1-dioxide (2) affords a useful synthesis of ethanesulfinates with the following functions in the 2-position: thiol, disulfide, trisulfide, thiosulfate, thiosulfonate, and phosphorothioate.The sulfinic esters generally were rather stable, but in several instances the salts gave unexpected results because of involvement of the sulfinate function with the sulfur atom of the 2-substituent; for example, the thiosulfonate p-MeC6H4SO2(CH2)2SO2Na (17) in water quickly liberated sodium p-toluenesulfinate (15) and gave an insoluble polymer shown by mass spectra to have the structure p-MeC6H4SO2nSO2Na (26).Aryl disulfides of the structure ArSS(CH2)2S(O)OMe were reasonably stable thermally but were quite sensitive to light.

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