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

32188-59-3

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32188-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32188-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,8 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32188-59:
(7*3)+(6*2)+(5*1)+(4*8)+(3*8)+(2*5)+(1*9)=113
113 % 10 = 3
So 32188-59-3 is a valid CAS Registry Number.

32188-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-bis(thiobenzyl)ethane

1.2 Other means of identification

Product number -
Other names acetaldehyde dibenzyldithioacetal

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:32188-59-3 SDS

32188-59-3Relevant academic research and scientific papers

Copper-catalyzed selective syntheses of Markovnikov-type hydrothiolation products and thioacetals by the reactions of thiols with alkenes bearing heteroatoms

Xi, Hui,Ma, Enlu,Li, Zhiping

, p. 4111 - 4116 (2016/07/06)

Catalyst-controlled divergent reactions of thiophenols with alkenes bearing heteroatoms have been developed. Markovnikov-type hydrothiolation products and thioacetals were synthesized selectively by switching copper catalysts.

The sulfohaloform reaction revisited and revised

Baum, James Clayton,Hardstaff, William Rayne,Langler, Richard Francis,Makkinje, Anthony

, p. 1687 - 1691 (2007/10/02)

A study of the aqueous chlorinolyses of a series of benzylic dithioacetals along with related α-chlorobenzylic sulfides is reported.These results require a modification of our previously proposed sulfohaloform reaction, so that thionium ion intermediates which have at least one alkyl group on sp2 carbon follow a different pathway.

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