N-Acetyl-L-phenylalanine丨CAS 2018-61-3

N-Acetyl-L-phenylalanine丨CAS 2018-61-3
Product Introduction:
CAS No.: 2018-61-3
Product Name: N-Acetyl-L-phenylalanine
Grade: AJI92
Molecular Formula: C11H13NO3
Molecular Weight: 207.23
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Technical Parameters
Description

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N-Acetyl-L-Phenylalanine is an N-acetylated derivative of L-phenylalanine, an aromatic amino acid with a benzyl side chain. Its defined L-configuration, aromatic structure, and acetylated amino group make it relevant to amino acid chemistry, biochemical research, and specialty organic synthesis. This compound may serve as a research material for investigating modified amino acids, molecular structure–property relationships, and the preparation of related chemical derivatives.

 

Chemical Identifiers

 

InChI InChI=1S/C11H13NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15)/t10-/m0/s1
InChI Key CBQJSKKFNMDLON-JTQLQIEISA-N
Smiles CC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)O
EC No. 217-959-8
MDL No. MFCD00063158
PubChem CID 74839

 

 

 

Applications

 

Pharmaceutical Research and Drug Discovery

Phenylalanine-based structures are investigated in medicinal chemistry because aromatic groups can contribute to molecular interactions and influence physicochemical properties. N-Acetyl-L-Phenylalanine may be considered in exploratory research involving modified amino acids and the development of structurally related compounds. Any pharmaceutical application requires experimental evaluation of the target molecule and should not be inferred from the compound's structure alone.

Biochemical and Amino Acid Research

N-Acetyl-L-Phenylalanine can support research involving chemically modified amino acids and their physicochemical properties. The L-configuration provides a defined stereochemical feature for studies comparing amino acid derivatives, while the N-acetyl group allows researchers to investigate the effects of amino-group modification on molecular behavior and chemical reactivity.

Organic Synthesis and Chemical Research

The aromatic side chain and carboxylic acid functionality make N-Acetyl-L-Phenylalanine relevant to synthetic chemistry research. It may be used as a starting material or intermediate in suitable synthetic pathways for preparing related phenylalanine derivatives and functionalized aromatic compounds. The feasibility of further transformations depends on the target structure, reaction conditions, and compatibility of the functional groups.

Analytical Chemistry and Method Development

N-Acetyl-L-Phenylalanine may be used in suitable analytical workflows involving amino acid derivatives and related aromatic compounds. Depending on its verified purity and characterization, it can support chromatographic separation, compound identification, and analytical method development. Applications requiring a reference standard should include appropriate identity verification, purity assessment, and qualification for the intended analytical purpose.

 

 

 

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