15080-35-0 Usage
Uses
Used in Scientific Research:
Phenylalanine, 4-chloro-a-methylis used as a research tool for studying the role of serotonin in various physiological and behavioral processes. It helps researchers understand the mechanisms and effects of serotonin in the body.
Used in Pharmaceutical Industry:
Phenylalanine, 4-chloro-a-methylis used as a potential therapeutic agent for the treatment of psychiatric disorders. Its ability to inhibit serotonin synthesis can be utilized to modulate neurotransmitter levels and alleviate symptoms associated with certain mental health conditions.
Used in Oncology Research:
Phenylalanine, 4-chloro-a-methylis used as a potential therapeutic agent in cancer research. Its inhibitory effect on serotonin synthesis may have implications for the treatment of certain types of cancer, as serotonin has been implicated in tumor growth and progression.
Used in Drug Development:
Phenylalanine, 4-chloro-a-methylis used in the development of new drugs targeting the serotonin pathway. Its ability to irreversibly inhibit tryptophan hydroxylase can be leveraged to create novel therapeutic agents for various conditions, including psychiatric disorders and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 15080-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15080-35:
(7*1)+(6*5)+(5*0)+(4*8)+(3*0)+(2*3)+(1*5)=80
80 % 10 = 0
So 15080-35-0 is a valid CAS Registry Number.
15080-35-0Relevant academic research and scientific papers
α-METHYL AMINO ACIDS BY CATALYTIC PHASE-TRANSFER ALKYLATIONS
O'Donnell, Martin J.,LeClef, Brigitte,Rusterholz, David B.,Ghosez, Leon,Antoine, Jean-Pierre,Navarro, Mirtha
, p. 4259 - 4262 (2007/10/02)
The α-methyl amino acids, α-methyl p-chlorophenylalanine, α-methyl p-tyrosine, α-methyl m-tyrosine and α-methyl DOPA have been prepared in good yields from amino ester hydrochlorides.The key step in the method is the catalytic phase-transfer alkylation of Schiff base derivatives of monoalkyl amino acids.
