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52162-05-7

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52162-05-7 Usage

General Description

S-Phenylhomocysteine is a chemical compound with the molecular formula C11H13NO3S. It is an amino acid derivative that contains a phenyl group and is structurally related to homocysteine. S-phenylhomocysteine is generated by the methylation of homocysteine and is a key intermediate in the biosynthesis of methionine. It has been studied for its potential role in cardiovascular health, as elevated levels of homocysteine have been associated with increased risk of cardiovascular disease. Research has also shown that S-phenylhomocysteine can inhibit the enzyme glycine N-methyltransferase, which is involved in the regulation of methionine metabolism. Additional studies are needed to fully understand the physiological and pathological implications of S-phenylhomocysteine in the human body.

Check Digit Verification of cas no

The CAS Registry Mumber 52162-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,6 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52162-05:
(7*5)+(6*2)+(5*1)+(4*6)+(3*2)+(2*0)+(1*5)=87
87 % 10 = 7
So 52162-05-7 is a valid CAS Registry Number.

52162-05-7SDS

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-amino-4-phenylsulfanylbutanoic acid

1.2 Other means of identification

Product number -
Other names DL-Homocysteine,S-phenyl

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:52162-05-7 SDS

52162-05-7Relevant articles and documents

Reaction of aziridinecarboxylic acids with thiols in aqueous solution. The formation of β-amino acid

Hata,Watanabe

, p. 3881 - 3888 (2007/10/02)

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