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Product Information

Product Name
Boc-L-glutamic acid g-benzyl ester
Brand Name
Chem Impex
Product Number
01349
CAS
13574-13-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
83589
IUPAC Name
(2S)-2-(2-methylpropan-2-yl)oxycarbonylamino-5-oxo-5-phenylmethoxypentanoic acid
InChI Key
AJDUMMXHVCMISJ-ZDUSSCGKSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CCC(=O)OCC1=CC=CC=C1)C(=O)O

Application

Boc-L-glutamic acid g-benzyl 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 that can be used in drug development and biological studies.

Drug Development: Its ability to modify amino acids makes it valuable in designing pharmaceuticals, particularly in developing compounds that target specific biological pathways.

Bioconjugation: The compound can be used in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents, enhancing their effectiveness and targeting capabilities.

Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is used in studies exploring the role of glutamate in the nervous system, aiding in the understanding of various neurological disorders.

Cosmetic Formulations: The compound is also being explored in cosmetic chemistry for its potential to improve skin hydration and elasticity, making it a candidate for anti-aging products.

References Data Source From Pubchem

Boc/Bzl Solid-Phase Synthesis of Deltorphin II and Its Analogs without the Utilization of Anhydrous Hydrogen Fluoride

Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2024-10
DOI: 10.1134/s1068162024050297

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

The best and the brightest: exploiting tryptophan-sensitized Tb(3+) luminescence to engineer lanthanide-binding tags

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2015
DOI: 10.1007/978-1-4939-2020-4_14

Peptidomimetics Through Click Chemistry: Synthesis of Novel β-Keto Triazole Acids from N-Protected Amino Acids

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2010-05-16
DOI: 10.1007/s10989-010-9214-z