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Sku CI02850_25_G
Chem Impex
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Product Information

Product Name
Boc-L-glutamic acid a-methyl ester
Brand Name
Chem Impex
Product Number
02850
CAS
72086-72-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7018754
IUPAC Name
(4S)-5-methoxy-4-(2-methylpropan-2-yl)oxycarbonylamino-5-oxopentanoic acid
InChI Key
ZAYAFKXUQMTLPL-ZETCQYMHSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CCC(=O)O)C(=O)OC

Application

Boc-L-glutamic acid a-methyl ester is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create specific sequences for various biological studies.

Drug Development: It plays a role in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing drug efficacy.

Bioconjugation: The chemical is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating research in diagnostics and therapeutics.

Protein Engineering: It is valuable in modifying proteins to improve their stability and functionality, which is crucial in fields like biotechnology and enzyme engineering.

Research on Neurotransmitters: The compound aids in studying glutamate receptors, contributing to advancements in understanding neurological disorders and developing potential treatments.

References Data Source From Pubchem

Synthesis of l-Kynurenine and Homo-l-Kynurenine via an Aza-Fries Rearrangement

Publication Name: Synthesis
Publication Date: 2020-08-06
DOI: 10.1055/s-0040-1707223

Propanephosphonic Acid Anhydride (T3P®) - A Benign Reagent for Diverse Applications Inclusive of Large-Scale Synthesis

Publication Name: Synthesis
Publication Date: 2013-06-03
DOI: 10.1055/s-0033-1338989

(Diacyloxyiodo)arenes from (Diacetoxyiodo)benzene by Ligand Exchange with a Carboxylic Acid

Publication Name: Science of Synthesis
Publication Date: 2007

Synthesis of Ring-A-Substituted Tryptophan by a Palladium-Catalyzed Heteroannulation Reaction

Publication Name: Synlett
Publication Date: 2005
DOI: 10.1055/s-2005-917079