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Benzenemethanethiol, 4-methoxy-α-phenyl-, also known as 4-methoxyphenylmethylmercaptan or 4-methoxybenzylmercaptan, is an organic compound with the chemical formula C8H10OS. It is a colorless to pale yellow liquid with a distinctive, strong odor. Benzenemethanethiol, 4-methoxy-a-phenyl- is characterized by the presence of a benzene ring, a methoxy group (-OCH3) at the para position, and a thiol group (-SH) attached to a methylene bridge (-CH2-). It is used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is typically handled with care and stored under controlled conditions to prevent unwanted reactions.

24677-21-2

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24677-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24677-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24677-21:
(7*2)+(6*4)+(5*6)+(4*7)+(3*7)+(2*2)+(1*1)=122
122 % 10 = 2
So 24677-21-2 is a valid CAS Registry Number.

24677-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl)phenylmethanethiol

1.2 Other means of identification

Product number -
Other names 4-Methoxy-benzhydrylmercaptan

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:24677-21-2 SDS

24677-21-2Relevant academic research and scientific papers

Enantioselective synthesis of tertiary thiols by intramolecular arylation of lithiated thiocarbamates

MacLellan, Paul,Clayden, Jonathan

supporting information; experimental part, p. 3395 - 3397 (2011/05/04)

Lithiation of N-aryl S-α-alkylbenzyl thiocarbamates leads to rearrangement with migration of the N-aryl ring to the anionic centre α to S, a process which generally proceeds with ca. 98% retention of stereochemistry and returns chiral benzylic tertiary thiols in high enantiomeric ratios.

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