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13046-50-9

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13046-50-9 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 90, p. 6554, 1968 DOI: 10.1021/ja01025a077

Check Digit Verification of cas no

The CAS Registry Mumber 13046-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13046-50:
(7*1)+(6*3)+(5*0)+(4*4)+(3*6)+(2*5)+(1*0)=69
69 % 10 = 9
So 13046-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12S4/c1-7-5(8-2)6(9-3)10-4/h1-4H3

13046-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2-tetrakis(methylsulfanyl)ethene

1.2 Other means of identification

Product number -
Other names Ethene, tetrakis(methylthio)-

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:13046-50-9 SDS

13046-50-9Relevant articles and documents

Electrochemical Reduction of Alkyl Aryl and Dialkyl Trithiocarbonates

Falsig, Mogens,Lund, Henning

, p. 545 - 550 (2007/10/02)

Electrochemical reduction in aprotic medium of alkyl aryl trithiocarbonates (1a-c) in the presence of an alkylating agent gives tetraalkyltetrathioethylenes (2a-c); under similar conditions dialkyl trithiocarbonates (3a-c) also form 2, but the reaction is complicated by the ability of 3 to act as an alkylating agent.The mechanisms of the reactions are discussed on the basis of the preparative and cyclic voltammetric results.

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