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Dithiocarbonic acid S-butyl ester S-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55716-07-9

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55716-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55716-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,1 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55716-07:
(7*5)+(6*5)+(5*7)+(4*1)+(3*6)+(2*0)+(1*7)=129
129 % 10 = 9
So 55716-07-9 is a valid CAS Registry Number.

55716-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name S-butylS-ethyl carbonodithioate

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:55716-07-9 SDS

55716-07-9Downstream Products

55716-07-9Relevant academic research and scientific papers

Thiyl radicals in gas-phase thermolysis of xanthic acid esters

Deryagina,Korchevin,Russavskaya,Sukhomazova,Levanova

, p. 140 - 143 (1996)

Gas-phase thermolysis of xanthic acid esters and their reaction with acetylene at 250-600°C have been studied for the first time. The direction of the thermolysis is determined by the nature of the substituents at the oxygen and sulfur atoms. The main products of the thermolysis are gaseous hydrocarbons, carbon monoxide and hydrogen sulfide. The yields of liquid products of the thermolysis and of the reactions with acetylene are 4-46 %. The role of thiyl radicals in thiophene molecule formation and reaction routes to carbon disulfide, dithiocarbonates, and stilbene are discussed.

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