54631-37-7 Usage
Uses
Used in Pharmaceutical Industry:
L-Phenylglycine hydrochloride is utilized as a chiral building block for the synthesis of pharmaceutical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure drugs, which is crucial for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Agrochemical Industry:
(S)-2-amino-4-oxo-4-phenylbutanoic acid hydrochloride also serves as a precursor in the synthesis of agrochemicals, specifically antibacterial and antifungal agents. Its incorporation into these products enhances their effectiveness in controlling and preventing infections in crops, thereby contributing to increased agricultural productivity.
Used in Material Development:
L-Phenylglycine hydrochloride has potential applications in the development of new materials. Its unique chemical properties and reactivity make it a valuable component in the creation of innovative materials with specific characteristics for various industries.
Used in Chemical Research:
As a versatile chemical compound, L-Phenylglycine hydrochloride is also employed in chemical research. It serves as a model compound for studying various chemical reactions and mechanisms, contributing to the advancement of knowledge in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 54631-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,3 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54631-37:
(7*5)+(6*4)+(5*6)+(4*3)+(3*1)+(2*3)+(1*7)=117
117 % 10 = 7
So 54631-37-7 is a valid CAS Registry Number.
54631-37-7Relevant academic research and scientific papers
Synthesis of α-Amino Acids by Reaction of t-Butyl N-(t-Butoxycarbonyl)iminoacetate With C-Nucleophiles
Muenster, Peter,Steglich, Wolfgang
, p. 223 - 225 (2007/10/02)
The reaction of t-butyl N-(t-butoxycarbonyl)iminoacetate with Grignard reagents or enamines yields N-(t-butoxycarbonyl)amino acid t-butyl esters which can be easily converted into the free amino acids by treatment with acids.
