64231-54-5 Usage
Uses
Used in Pharmaceutical Industry:
4-FLUORO-L-PHENYLALANINE HYDROCHLORIDE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs targeting a range of medical conditions. Its unique structure allows for the creation of molecules with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic chemistry, 4-FLUORO-L-PHENYLALANINE HYDROCHLORIDE is utilized as a versatile building block for the creation of complex organic compounds. Its presence can influence the reactivity and selectivity of synthetic pathways, facilitating the production of desired molecules.
Used in Research and Development:
4-FLUORO-L-PHENYLALANINE HYDROCHLORIDE is employed as a valuable tool in research and development settings. It aids scientists in understanding the effects of fluorination on biological activity and serves as a starting material for exploring novel chemical entities with potential therapeutic benefits.
Used in Drug Discovery:
4-FLUORO-L-PHENYLALANINE HYDROCHLORIDE is used in drug discovery processes to identify and optimize lead compounds. Its incorporation into molecular structures can enhance pharmacokinetic and pharmacodynamic properties, leading to the development of more effective and safer medications.
Check Digit Verification of cas no
The CAS Registry Mumber 64231-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,3 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64231-54:
(7*6)+(6*4)+(5*2)+(4*3)+(3*1)+(2*5)+(1*4)=105
105 % 10 = 5
So 64231-54-5 is a valid CAS Registry Number.
64231-54-5Relevant academic research and scientific papers
UNUSUAL AMINO ACIDS II. Asymmetric Synthesis of Fluorine Containing Phenylalanines
Krause, Hans-Walter,Kreuzfeld, Hans-Joern,Doebler, Christian,Taudien, Stefan
, p. 555 - 566 (2007/10/02)
Few (Z)-α-N-benzoylamino-β-(fluorophenyl)-acrylic acids and their esters were prepared by known procedures and hydrogenated to the corresponding optically active α-benzoyl-β-(fluorophenyl)-alanine derivatives with optical yields up to 90percent using the
