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
123053-22-5Relevant 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