74164-07-1 Usage
Uses
Used in Pharmaceutical Research:
N-benzoyl-2-chloro-phenylalanine is used as a building block for the synthesis of peptides and proteins, contributing to the development of new drugs and therapeutic agents. Its benzoyl and 2-chloro modifications provide selective chemical modification sites, enhancing the compound's utility in pharmaceutical applications.
Used in Biochemical Studies:
In the field of biochemistry, N-benzoyl-2-chloro-phenylalanine is employed to understand the structure and function of biological molecules. Its unique properties allow researchers to study the effects of specific modifications on the behavior and interactions of peptides and proteins.
Used in Drug Development:
N-benzoyl-2-chloro-phenylalanine is used as a key component in the development of new drugs, particularly those targeting specific biological pathways or molecular interactions. Its stability and reactivity make it an ideal candidate for creating novel therapeutic agents with potential applications in various medical fields.
Used in Chemical Modification of Biomolecules:
N-benzoyl-2-chloro-phenylalanine is also used for the chemical modification of biomolecules, such as proteins and peptides, to study their structure, function, and interactions with other molecules. This application is crucial for advancing our understanding of biological processes and developing targeted therapies for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 74164-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74164-07:
(7*7)+(6*4)+(5*1)+(4*6)+(3*4)+(2*0)+(1*7)=121
121 % 10 = 1
So 74164-07-1 is a valid CAS Registry Number.
74164-07-1Relevant academic research and scientific papers
Synthesis of Acylamino Acids and Acylamino Acid Amides by Simultaneous Reduction and Hydrolysis of Unsaturated 2,4-Disubstituted 2-Imidazolin-5-ones
Devasia, Ganapathiplackal M.,Shafi, P. Mohamed
, p. 204 - 206 (2007/10/02)
Twelve acylamino acids (II) and two acylamino acid amides (III) have been prepared by the simultaneous reduction and hydrolysis of unsaturated 2,4-disubstituted 2-imidazolin-5-ones (I) with a mixture of zinc dust and potassium hydroxide solution.
Synthesis of Acylamino Acid Amides and Acylamino Acids via 2,4-Disubstituted 2-Imidazolin-5-ones
Devasia, Ganapathiplackal M.,Shafi, P. Mohamed
, p. 70 - 72 (2007/10/02)
Unsaturated 2,4-disubstituted 2-imidazolin-5-ones (I) have been reduced with a mixture of hydriodic acid and red phosphorus in the presence of acetic anhydride to give the saturated 2,4-disubstituted 2-imidazolin-5-ones (II) which have been hydrolysed to acylamino acid amides (III) and acylamino acids (IV) with sodium hydroxide solution under different conditions.In all six acylamino acid amides (23 - 51percent yields) and four acylamino acids (26 - 65percent yields) have been prepared.One saturated 2-imidazolin-5-one, namely 2-phenyl-4-benzyl-2-imidazolin-5-one has been isolated from the reaction in 40percent yield and identified.
