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Sku CI11818_1_G
Chem Impex
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Product Information

Product Name
Boc-L-alanine methyl ester
Brand Name
Chem Impex
Product Number
11818
CAS
28875-17-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
10856577
IUPAC Name
methyl (2S)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoate
InChI Key
GJDICGOCZGRDFM-LURJTMIESA-N
SMILES
CC@@H(C(=O)OC)NC(=O)OC(C)(C)C

Description

Boc-L-alanine 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 chemists to create complex structures for pharmaceuticals and research applications.

Drug Development: Its role in modifying amino acids makes it valuable in the development of new drugs, particularly in designing compounds that can enhance bioavailability and efficacy.

Bioconjugation: The protective Boc group allows for selective reactions in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies.

Research in Neuroscience: Used in the synthesis of neurotransmitter analogs, it helps researchers explore neurological pathways and develop treatments for disorders.

Custom Synthesis Services: Many chemical suppliers offer custom synthesis of Boc-L-alanine methyl ester, catering to specific research needs, thus providing flexibility for researchers in various fields.

References Data Source From Pubchem

Boron clusters as efficient shuttles for electrocatalytic deuterium labelling via radical H/D exchange

Publication Name: Nature Catalysis
Publication Date: 2025-07-15
DOI: 10.1038/s41929-025-01379-6

Total Synthesis of Endolides A and B

Publication Name: Synlett : accounts and rapid communications in synthetic organic chemistry
Publication Date: 2019-11-14
DOI: 10.1055/s-0037-1610736

Hydrogenation of Optically Active Esters

Publication Name: Science of Synthesis
Publication Date: 2017

3-(1-Aminoalkyl)pyrazole- and 4,5-Dihydropyrazole-5-carboxylic Acids as Peptide Bond Replacements

Publication Name: Synlett
Publication Date: 2011-01
DOI: 10.1055/s-0030-1259303