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2-Allylbenzenethiol, also known as 2-(2-propenyl)benzenethiol or 2-allylthiophenol, is an organic compound with the chemical formula C9H10S. It is a colorless to pale yellow liquid with a strong, pungent odor. This sulfur-containing aromatic compound is characterized by a benzene ring with a thiol group (-SH) at the 2-position and an allyl group (CH2=CHCH2-) attached to the same carbon. 2-Allylbenzenethiol is used as a synthetic intermediate in the production of various chemicals, such as pharmaceuticals, agrochemicals, and fragrances. It is also employed as a reagent in organic synthesis and as a building block for the preparation of more complex molecules. Due to its reactive nature, it is essential to handle 2-allylbenzenethiol with care, as it can cause skin and respiratory irritation.

6165-54-4

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6165-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6165-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6165-54:
(6*6)+(5*1)+(4*6)+(3*5)+(2*5)+(1*4)=94
94 % 10 = 4
So 6165-54-4 is a valid CAS Registry Number.

6165-54-4Downstream Products

6165-54-4Relevant academic research and scientific papers

The Mechanism of Catalysis of the Thio-Claisen Rearrangement

Kwart, H.,Miles, W. H.,Horgan, A. G.,Kwart, L. D.

, p. 1757 - 1760 (1981)

The cyclization-induced rearrangement mechanism proposed by Overman to account for nucleophilc catalysis of the thio-Claisen rearrangement has been tested by application of two criteria, viz., the secondary kinetic deuterium isotope effect at the β (side

Catalyst free annulative thioboration of unfunctionalized olefins

Yang, Zhantao,Yang, Chun-Hua,Chen, Shiqi,Chen, Xixi,Zhang, Litian,Ren, Huijun

supporting information, p. 12092 - 12095 (2017/11/14)

A direct and catalyst-free annulative thioboration of unfunctionalized olefins has been developed. In the presence of BCl3 as the sole boron source, the boryl group and thiol group are added to the C-C double bonds simultaneously. The boronic acids obtained can be protected to form synthetically ubiquitous pinacol boronate esters.

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