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3-chloro-1-octenyl-1,1-bis thiobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

198982-71-7

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198982-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198982-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,9,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 198982-71:
(8*1)+(7*9)+(6*8)+(5*9)+(4*8)+(3*2)+(2*7)+(1*1)=217
217 % 10 = 7
So 198982-71-7 is a valid CAS Registry Number.

198982-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-1-octenyl-1,1-bis thiobenzene

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:198982-71-7 SDS

198982-71-7Downstream Products

198982-71-7Relevant academic research and scientific papers

Synthesis of α,β-unsaturated aldehydes and methyl carboxylic esters from 2-acetylenic phenyl sulfides

Fortes, Carlos C.,Garrote, Clevia F. D.

, p. 3917 - 3941 (2007/10/03)

2-Alkynylthio benzenes were reduced to 2-Alkenylthio benzenes with diisobutyl aluminum hydride. Mono chlorination of these compounds with sulfuryl chloride and pyridine followed by hydrolysis, in the presence of Cu(II) salts, gave α,β-unsaturated aldehydes. 2-Alkynylthio benzenes were converted into 2-Alkynyl 1,1-bis thiobenzenes by monochlorination with sulfuryl chloride and pyridine followed by treatment with thiophenol and triethylamine. These substances were then converted to α,β-unsaturated methyl carboxylic esters by way of isomerization with sodium methoxide to the corresponding allene and treatment with hydrochloric acid and methanolysis in the presence of iodine.

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