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Bis[(4-methylphenyl)sulfanyl]acetic acid, a chemical compound with the molecular formula C16H16O4S2, is a white to off-white crystalline powder. It has a molecular weight of 336.42 g/mol and is known for its potential therapeutic properties, including anti-inflammatory and analgesic effects. This makes it a promising candidate for developing new drugs and a valuable component in the field of organic chemistry.

17067-32-2

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17067-32-2 Usage

Uses

Used in Pharmaceutical Industry:
Bis[(4-methylphenyl)sulfanyl]acetic acid is used as a pharmaceutical intermediate for its anti-inflammatory and analgesic effects, making it a promising candidate for developing new drugs.
Used in Organic Chemistry:
Bis[(4-methylphenyl)sulfanyl]acetic acid is used as a building block in the synthesis of other organic compounds, contributing to the development of various chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17067-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17067-32:
(7*1)+(6*7)+(5*0)+(4*6)+(3*7)+(2*3)+(1*2)=102
102 % 10 = 2
So 17067-32-2 is a valid CAS Registry Number.

17067-32-2SDS

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 2,2-bis[(4-methylphenyl)sulfanyl]acetic acid

1.2 Other means of identification

Product number -
Other names bis-p-tolylsulfanyl-acetic acid

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:17067-32-2 SDS

17067-32-2Relevant academic research and scientific papers

Novel Alumina-catalysed Reactions of Arylthioalkyl Halides and Related Compounds

Jigajinni, Veerappa B.,Wightman, Richard H.

, p. 1801 - 1812 (2007/10/02)

Arylthioalkyl halides of the type ArS(CH2)nCl (Ar = phenyl or substituted phenyl, n = 1-4) undergo rearrangement on heating with neutral alumina to 1,n-bis(arylthio)alkanes of type ArS(CH2)nSAr in high yield.Similar rearrangements occur with some closely related structural types.The bis(arylthio)alkanes undergo further reaction with alumina at higher temperatures in air giving diaryl disulphides.Bis(o-iodophenylthio)methane eliminates iodine on heating with alumina, producing dibenzodithiepin.Some observations concerning the mechanism are presented.

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