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Sku CI06552_1_G
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Product Information

Product Name
Z-L-phenylalanine methyl ester
Brand Name
Chem Impex
Product Number
06552
CAS
35909-92-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
3082435
IUPAC Name
methyl (2S)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoate
InChI Key
BBACSHIJBOGXKL-INIZCTEOSA-N
SMILES
COC(=O)C@H(CC1=CC=CC=C1)NC(=O)OCC2=CC=CC=C2

Application

Z-L-phenylalanine methyl ester is widely utilized in research focused on

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create biologically active compounds.

Drug Development: It is used in the development of new drugs, especially those targeting neurological conditions, due to its ability to influence neurotransmitter activity.

Biochemical Research: Researchers employ this chemical in studies related to enzyme activity and protein interactions, providing insights into metabolic pathways.

Cosmetic Formulations: The compound is incorporated into skincare products for its potential benefits in skin health, acting as a moisturizing agent.

Food Industry: It is also explored for flavor enhancement in food products, leveraging its amino acid properties to improve taste profiles.

References Data Source From Pubchem

Transesterification of α-Amino Esters Catalyzed by a Tetranuclear Zinc Cluster: Zn4(OCOCF3)6O

Publication Name: Synlett
Publication Date: 2011-12-09
DOI: 10.1055/s-0031-1290096

Versatile Selective α-Carboxylic Acid Esterification of N-Protected Amino Acids and Peptides by Alcalase

Publication Name: Synthesis
Publication Date: 2009-02-11
DOI: 10.1055/s-0028-1083362

Asymmetric Hydrogenation

Publication Name: Science of Synthesis
Publication Date: 2005

Conversion of Carbamates

Publication Name: Science of Synthesis
Publication Date: 2005

Protease-catalyzed peptide synthesis for the site-specific incorporation of alpha-fluoroalkyl amino acids into peptides

Publication Name: The Journal of Organic Chemistry
Publication Date: 2003-02-27
DOI: 10.1021/jo020613p