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2-(Hexadecylthio)benzoic acid is a chemical compound with the molecular formula C23H36O2S. It is an organic compound that belongs to the class of benzoic acids, characterized by the presence of a hexadecylthio group (a 16-carbon alkyl chain with a sulfur atom) attached to the 2-position of the benzene ring. 2-(Hexadecylthio)benzoic acid is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, where it may be used as an intermediate in the synthesis of other compounds or as a functional group in the development of new materials. Its specific properties and reactivity are influenced by the combination of the aromatic benzoic acid structure and the hydrophobic, sulfur-containing alkyl chain.

2182-24-3

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2182-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2182-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2182-24:
(6*2)+(5*1)+(4*8)+(3*2)+(2*2)+(1*4)=63
63 % 10 = 3
So 2182-24-3 is a valid CAS Registry Number.

2182-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hexadecylthio)benzoic acid

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

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More Details:2182-24-3 SDS

2182-24-3Relevant academic research and scientific papers

Lipase-catalyzed kinetic resolution of a series of esters having a sulfoxide group as the stereogenic centre

Allenmark,Andersson

, p. 2371 - 2376 (2007/10/02)

A series of methyl 2-(alkylsulfinyl)benzoates (alkyl = C1, n-C4, n-C8, n-C12 and n-C16) was investigated with respect to substrate behaviour and enantioselectivity in a lipase (Candida rugosa)-catalyz

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