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Benzenemethanethiol, 2,4,6-tris(1,1-dimethylethyl)-α-methyl, also known as 2,4,6-trimethylbenzylmercaptan, is an organic compound with the chemical formula C13H22S. It is a colorless to pale yellow liquid with a strong, pungent odor. Benzenemethanethiol, 2,4,6-tris(1,1-dimethylethyl)-a-methyl- is characterized by its unique structure, featuring a benzene ring with three methyl groups at the 2, 4, and 6 positions, and a methyl group attached to the α-carbon of a methanethiol (mercaptan) group. It is used in the synthesis of various organic compounds and as a chemical intermediate in the pharmaceutical and agrochemical industries. Due to its strong odor, it is also used as a scent component in perfumery.

89738-80-7

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89738-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89738-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,3 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89738-80:
(7*8)+(6*9)+(5*7)+(4*3)+(3*8)+(2*8)+(1*0)=197
197 % 10 = 7
So 89738-80-7 is a valid CAS Registry Number.

89738-80-7SDS

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 1-(2,4,6-Tri-tert-butyl-phenyl)-ethanethiol

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

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More Details:89738-80-7 SDS

89738-80-7Downstream Products

89738-80-7Relevant academic research and scientific papers

REACTIONS OF A STABLE THIOBENZALDEHYDE WITH ORGANOMETALLICS

Okazaki, Renji,Fukuda, Nobuo,Oyama, Hiroyuki,Inamoto, Naoki

, p. 101 - 104 (2007/10/02)

Rections of 2,4,6-tri-t-butylthiobenzaldehyde with Grignard and organolithium reagents gave products via the anion radical of the thioaldehyde.The first example of dimerization of thioketyl radicals was also presented.

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