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Benzenemethanethiol, 2-methyl-α-phenyl, also known as 2-Methylbenzyl Mercaptan or 2-Methylbenzyl Mercaptide, is an organic compound with the chemical formula C8H10S. It is a colorless to pale yellow liquid with a strong, unpleasant odor. Benzenemethanethiol, 2-methyl-a-phenyl- is primarily used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also employed as a fragrance ingredient in the perfume industry. Due to its reactive nature, it is essential to handle Benzenemethanethiol, 2-methyl-a-phenyl- with care, as it can cause irritation to the eyes, skin, and respiratory system.

97841-23-1

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97841-23-1 Usage

Chemical compound

Benzenemethanethiol, 2-methyl-a-phenyl

Physical appearance

Colorless to pale yellow liquid

Odor

Strong, unpleasant odor similar to rotten cabbage

Uses

Production of various chemicals including pharmaceuticals, fragrances, pesticides; flavoring agent in the food industry

Handling precautions

Harmful if inhaled, ingested, or in contact with skin; should be used in a well-ventilated area and with appropriate personal protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 97841-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97841-23:
(7*9)+(6*7)+(5*8)+(4*4)+(3*1)+(2*2)+(1*3)=171
171 % 10 = 1
So 97841-23-1 is a valid CAS Registry Number.

97841-23-1Upstream product

97841-23-1Downstream Products

97841-23-1Relevant academic research and scientific papers

THE SOMMELET TYPE REARRANGEMENT OF CERTAIN TRITHIOORTHOESTTERS

Ikehira, Hideyuki,Tanimoto, Shigeo

, p. 7 - 16 (2007/10/02)

The carbanions produced by deprotonation at the carbon of methylthio group of 2-methylthio-2-phenyl-1,3-dithiane and of 4,6-dithia-5-methylthio-5-phenylnonane undergo the Sommelet type rearrangement to give intermediary thiolate anions which, on further d

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