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190841-64-6

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190841-64-6 Usage

Structure

Dithiol derivative with a biphenyl backbone and two thiol groups

Odor

Strong

Usage

Commonly used in organic synthesis and chemical research

Potential applications

a. Material science
b. Nanotechnology
c. Development of new sensor and electronic devices

Possible properties

a. Antioxidant
b. Anti-inflammatory

Research potential

Target for pharmaceutical research and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 190841-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,8,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190841-64:
(8*1)+(7*9)+(6*0)+(5*8)+(4*4)+(3*1)+(2*6)+(1*4)=146
146 % 10 = 6
So 190841-64-6 is a valid CAS Registry Number.

190841-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-(3-methyl-2-sulfanylphenyl)benzenethiol

1.2 Other means of identification

Product number -
Other names 1,1-Biphenyl-2,2-dithiol,3,3-dimethyl

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:190841-64-6 SDS

190841-64-6Upstream product

190841-64-6Relevant articles and documents

Synthesis of structurally modified atropisomeric biaryl dithiols. Observations on the Newman-Kwart rearrangement

Cossu, Sergio,De Lucchi, Ottorino,Fabbri, Davide,Valle, Giovanni,Painter, Gavin F.,Smith, Robin A.J.

, p. 6073 - 6084 (2007/10/03)

The preparation of a number of biaryldithiols from biaryldiols is discussed. A key reaction is the Newman-Kwart thermorearrangement of bisthiocarbamates and crucial variables of temperature and reaction time have been identified. Alternative approaches to 3,3'-disubstituted dithiols via ortho metallation are presented. The benefit of using such disubstituted compounds is illustrated with representative examples of the stereochemical features of the derived carbanions in reactions with prochiral electrophiles.

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