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1,1'-Biphenyl, 2-methyl-2'-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38351-01-8

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38351-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38351-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38351-01:
(7*3)+(6*8)+(5*3)+(4*5)+(3*1)+(2*0)+(1*1)=108
108 % 10 = 8
So 38351-01-8 is a valid CAS Registry Number.

38351-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-(2-methylsulfanylphenyl)benzene

1.2 Other means of identification

Product number -
Other names 2-Methyl-2'(methylthio)biphenyl

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:38351-01-8 SDS

38351-01-8Downstream Products

38351-01-8Relevant academic research and scientific papers

Regiochemistry and Stereochemistry of Nickel-Promoted, Carbon-Carbon Bond-Forming Reactions of Cyclic Sulfur Compounds

Tiecco, Marcello,Tingoli, Marco,Wenkert, Ernest

, p. 3828 - 3831 (1985)

Reaction of methylmagnesium iodide and phenylmagnesium bromide with thianaphthene, dibenzothiophenone, thianthrene, and 2,3-dihydrothiapyran in the presence of nickel dichloride have been shown to yield, regioselectively in most cases, ring-opened products in which the carbon-sulfur bonds have been replaced by carbon-carbon bonds.Stereospecific carbon-carbon bond formation has taken place in the reactions of thianaphthene and 2,3-dihydrothiapyran, the products having maintained the cis-olefin configuration of the starting sulfur compounds.Isomerization into the more stable compounds has been observed in some cases.

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