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Benzene, 1,1',1'',1'''-[1,2-ethenediylidenetetrakis(thiomethylene)]tetrakis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13046-51-0

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13046-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13046-51-0 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 13046-51:
(7*1)+(6*3)+(5*0)+(4*4)+(3*6)+(2*5)+(1*1)=70
70 % 10 = 0
So 13046-51-0 is a valid CAS Registry Number.

13046-51-0SDS

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 tetrakis(benzylthio)ethylene

1.2 Other means of identification

Product number -
Other names tetraki(benzylthio)ethylene

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:13046-51-0 SDS

13046-51-0Downstream Products

13046-51-0Relevant academic research and scientific papers

A facile synthesis of bis(ethylenedithio)tetrathiafulvalene

Muller,Ueba

, p. 853 - 854 (2007/10/02)

5,6-Dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-one (3) was prepared in one step starting from thiapendione (1; [1,3]dithiolo[4,5-d][1,3]dithiole-2,5-dione) in 55% yield via 4,5-dimercapto-1,3-dithiol-2-one (2). Coupling of 3 in triethyl phosphite gave bis(

Electrochemical Synthesis of Tetrathioethylenes

Falsig, Mogens,Lund, Henning

, p. 591 - 596 (2007/10/02)

Electrochemical reduction of 4,5-bis(alkylthio)-1,3-dithiol-2-ones (1a-d) in aprotic medium, followed by alkylation, gives tetrathioethylenes (2) in nearly quantitative yield.A similar reduction and alkylation of 1,3,4,6-tetrathiapentalene-2,5-dione (3) leads to 1 in almost quantitative yield. 4,5-Bis(alkylthio)-1,3-dithiole-2-thiones (4) gives tetrathiooethylenes under similar conditions in lower yield than 1.The mechanism of the reactions is discussed on the basis of the preparative and cyclic voltammetric results.

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