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Chem Impex
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Product Information

Product Name
Boc-D-a-tert-butylglycine
Brand Name
Chem Impex
Product Number
01354
CAS
124655-17-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7005057
IUPAC Name
(2R)-3,3-dimethyl-2-(2-methylpropan-2-yl)oxycarbonylaminobutanoic acid
InChI Key
LRFZIPCTFBPFLX-ZETCQYMHSA-N
SMILES
CC(C)(C)C@H(C(=O)O)NC(=O)OC(C)(C)C

Application

Boc-D-a-tert-butylglycine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial in developing complex peptides for pharmaceuticals.

Drug Development: Its unique structure aids in the design of new drugs, particularly in creating compounds with improved bioavailability and stability. Researchers can leverage its properties to enhance therapeutic efficacy.

Bioconjugation: Boc-D-a-tert-butylglycine is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules. This is particularly beneficial in the development of targeted drug delivery systems.

Protein Engineering: It plays a role in protein engineering, where it can be incorporated into proteins to study structure-function relationships. This helps in understanding protein interactions and designing better enzymes or antibodies.

Research in Neuroscience: Its derivatives are explored in neuroscience research for potential applications in neuroprotective agents, aiding in the development of treatments for neurodegenerative diseases.

References Data Source From Pubchem

Dipeptide Alkylphosphonium Salts with an Amide Moiety

Publication Name: Science of Synthesis
Publication Date: 2022

Cyanation Using Chiral Thioureas as Catalysts

Publication Name: Science of Synthesis
Publication Date: 2013

Enantioselective Reactions

Publication Name: Science of Synthesis
Publication Date: 2012

Gram-Scale Strecker Synthesis of Unnatural α-Amino Acids

Publication Name: Synfacts
Publication Date: 2009-12-21
DOI: 10.1055/s-0029-1218492