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Sku CI01348_5_G
Chem Impex
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Product Information

Product Name
Boc-L-glutamic acid-a-benzyl ester
Brand Name
Chem Impex
Product Number
01348
CAS
30924-93-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
153708
IUPAC Name
(4S)-4-(2-methylpropan-2-yl)oxycarbonylamino-5-oxo-5-phenylmethoxypentanoic acid
InChI Key
CVZUKWBYQQYBTF-ZDUSSCGKSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CCC(=O)O)C(=O)OCC1=CC=CC=C1

Application

Boc-L-glutamic acid-a-benzyl 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 creating protected amino acids that facilitate the formation of complex peptide chains.

Drug Development: It plays a significant role in medicinal chemistry, aiding in the design of new pharmaceuticals by modifying bioactive compounds to enhance their efficacy and stability.

Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving targeted delivery and therapeutic outcomes.

Research in Neuroscience: Its derivatives are explored for their potential in studying neurotransmitter pathways, contributing to the understanding of various neurological disorders.

Cosmetic Formulations: The compound is also being investigated for use in cosmetic products, where it can enhance skin penetration and improve the stability of active ingredients.

References Data Source From Pubchem

Symplocamide A as marine-derived proteasome inhibitor: a promising scaffold for targeted cancer therapy

Publication Name: Medical oncology (Northwood, London, England)
Publication Date: 2025-07-19
DOI: 10.1007/s12032-025-02870-7

Cadmium decreases the levels of glutathione and enhances the phytochelatin concentration in the marine dinoflagellate Lingulodinium polyedrum

Publication Name: Journal of Applied Phycology
Publication Date: 2016-08-20
DOI: 10.1007/s10811-016-0927-z

Challenges in the Syntheses of Peptidic Natural Products

Publication Name: Synthesis
Publication Date: 2012-05-25
DOI: 10.1055/s-0031-1289765

Straightforward Method for the Synthesis of Selenocysteine and Selenocystine Derivatives from l-Serine Methyl Ester

Publication Name: Synthesis
Publication Date: 2010-07-22
DOI: 10.1055/s-0030-1258188