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N-(N-benzyloxycarbonyl-L-leucyl)-L-phenylalanine benzyl ester is a chemical compound derived from the amino acids leucine and phenylalanine, which are essential for protein synthesis and cell function. N-(N-benzyloxycarbonyl-L-leucyl)-L-phenylalanine benzyl ester is characterized by the presence of a benzyl ester group attached to the phenylalanine amino acid, which provides stability and protection during chemical reactions. It is a versatile molecule with significant applications in pharmaceutical research, production, and the synthesis of peptides and proteins.

103365-03-3

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103365-03-3 Usage

Uses

Used in Pharmaceutical Research and Production:
N-(N-benzyloxycarbonyl-L-leucyl)-L-phenylalanine benzyl ester is used as a substrate for enzymatic reactions in the field of pharmaceutical research and production. Its role as a substrate allows for the study and manipulation of enzyme activity, which is crucial for understanding biological processes and developing new drugs.
Used in Peptide and Protein Synthesis:
As a building block, N-(N-benzyloxycarbonyl-L-leucyl)-L-phenylalanine benzyl ester is employed in the synthesis of peptides and proteins. Its structural properties make it a valuable component in the creation of complex molecular structures, contributing to the development of novel therapeutic agents and bioactive compounds.
Used in Drug Development:
This chemical compound is also utilized in the development of pharmaceutical drugs. Its unique structure and properties enable the design and synthesis of new drug candidates with potential therapeutic applications, particularly in the treatment of various diseases and conditions.
Used in Biochemistry and Molecular Biology Research:
N-(N-benzyloxycarbonyl-L-leucyl)-L-phenylalanine benzyl ester serves as a valuable tool in biochemistry and molecular biology research. It aids in the investigation of cellular processes, protein interactions, and the mechanisms underlying various biological functions, ultimately contributing to a deeper understanding of life sciences and the advancement of medical knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 103365-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103365-03:
(8*1)+(7*0)+(6*3)+(5*3)+(4*6)+(3*5)+(2*0)+(1*3)=83
83 % 10 = 3
So 103365-03-3 is a valid CAS Registry Number.

103365-03-3Upstream product

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