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123053-22-5

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123053-22-5 Usage

General Description

L-3-Chlorophenylalanine is a chemical compound that is a derivative of the amino acid phenylalanine. It is classified as a halogenated phenylalanine, and its molecular structure includes a chlorine atom attached to the third carbon of the phenylalanine molecule. L-3-Chlorophenylalanine is a potent inhibitor of the enzyme phenylalanine hydroxylase, which is involved in the metabolism of phenylalanine. L-3-CHLOROPHENYLALANINE has been used in scientific research to study the effects of altered phenylalanine metabolism, as well as to investigate the role of phenylalanine hydroxylase in various physiological processes. Additionally, L-3-Chlorophenylalanine has been implicated in the regulation of neurotransmitter levels in the brain, making it a potentially valuable tool for understanding neurological disorders and developing new therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 123053-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123053-22:
(8*1)+(7*2)+(6*3)+(5*0)+(4*5)+(3*3)+(2*2)+(1*2)=75
75 % 10 = 5
So 123053-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClNO2/c10-7-3-1-2-6(4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m1/s1

123053-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name L-3-CHLOROPHENYLALANINE

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:123053-22-5 SDS

123053-22-5Downstream Products

123053-22-5Relevant articles and documents

synthesis of both enantiomers of chiral phenylalanine derivatives catalyzed by cinchona alkaloid quaternary ammonium salts as asymmetric phase transfer catalysts

Jin, Lei,Zhao, Shuai,Chen, Xin

, (2018)

A practical synthesis of both enantiomers of unnatural phenylalanine derivatives by using two pseudoenantiomeric phase transfer catalysts is described. Through asymmetric α-alkylation of glycine Schiff base with substituted benzyl bromides and 1-(bromomet

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