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Sku CI03019_1_G
Chem Impex
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Product Information

Product Name
Benzoyl-L-alanine methyl ester
Brand Name
Chem Impex
Product Number
03019
CAS
7244-67-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
6364617
IUPAC Name
methyl (2S)-2-benzamidopropanoate
InChI Key
QRDFLIILGVFYCF-QMMMGPOBSA-N
SMILES
CC@@H(C(=O)OC)NC(=O)C1=CC=CC=C1

Description

Benzoyl-L-alanine methyl ester is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in creating analgesics and anti-inflammatory drugs.

Peptide Synthesis: It is often used in solid-phase peptide synthesis, enhancing the efficiency of producing peptides for therapeutic applications.

Cosmetic Formulations: The compound is incorporated into skincare products for its potential to improve skin texture and hydration, making it valuable in the cosmetic industry.

Biochemical Research: Researchers utilize it to study protein interactions and enzyme activity, providing insights into metabolic pathways and disease mechanisms.

Flavor and Fragrance Industry: Its aromatic properties make it suitable for use in flavoring agents and fragrances, adding a pleasant scent to various products.

References Data Source From Pubchem

Microwave-Induced Inverse Peptide Synthesis

Publication Name: Synfacts
Publication Date: 2022-11-17
DOI: 10.1055/s-0042-1752347

4-(Dimethylamino)pyridine-Derived Catalysts

Publication Name: Science of Synthesis
Publication Date: 2022

A novel cucumisin-like serine protease from leaf of legume Canavalia ensiformis

Publication Name: Journal of Plant Biochemistry and Biotechnology
Publication Date: 2020-08-24
DOI: 10.1007/s13562-020-00578-5

The self-disproportionation of enantiomers (SDE) of amino acids and their derivatives

Publication Name: Amino Acids
Publication Date: 2019-03-22
DOI: 10.1007/s00726-019-02729-y

Self-disproportionation of Enantiomers of Enantiomerically Enriched Compounds

Publication Name: Differentiation of Enantiomers II
Publication Date: 2013
DOI: 10.1007/128_2013_434