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Sku CI00853_25_G
Chem Impex
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Product Information

Product Name
Boc-D-valine
Brand Name
Chem Impex
Product Number
00853
CAS
22838-58-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
637605
IUPAC Name
(2R)-3-methyl-2-(2-methylpropan-2-yl)oxycarbonylaminobutanoic acid
InChI Key
SZXBQTSZISFIAO-SSDOTTSWSA-N
SMILES
CC(C)C@H(C(=O)O)NC(=O)OC(C)(C)C

Application

Boc-D-valine is widely utilized in research focused on

Peptide Synthesis: This compound serves as a protecting group for amino acids in peptide synthesis, allowing chemists to build complex peptides with high specificity and yield.

Pharmaceutical Development: It plays a crucial role in the development of pharmaceuticals, particularly in creating drugs that target specific biological pathways, enhancing efficacy and reducing side effects.

Biotechnology: In biotechnology, Boc-D-valine is used in the production of modified proteins, which can improve their stability and activity in various applications, such as enzyme engineering.

Research in Drug Design: Researchers utilize this compound in drug design studies to explore new therapeutic agents, particularly in the field of cancer treatment, where targeted therapies are essential.

Academic Research: It is frequently employed in academic laboratories for studies related to protein structure and function, helping scientists understand the role of amino acids in biological systems.

References Data Source From Pubchem

Synthesis of planar chiral ferrocenes via enantioselective remote C–H activation

Publication Name: Nature Chemistry
Publication Date: 2023-04-17
DOI: 10.1038/s41557-023-01176-3

Palladium-Catalyzed Stereoselective C–H Olefination of Biaryls

Publication Name: Synfacts
Publication Date: 2017-05-16
DOI: 10.1055/s-0036-1590495

Stereoisomeric Prodrugs to Improve Corneal Absorption of Prednisolone: Synthesis and In Vitro Evaluation

Publication Name: AAPS PharmSciTech
Publication Date: 2015-09-03
DOI: 10.1208/s12249-015-0400-3

Design and synthesis of mono and bicyclic tetrapeptides thioester as potent inhibitor of histone deacetylases

Publication Name: Amino Acids
Publication Date: 2014-07-22
DOI: 10.1007/s00726-014-1800-5

Total Synthesis of the Proposed Structure for Itralamide B

Publication Name: Synlett
Publication Date: 2014-03-14
DOI: 10.1055/s-0033-1340872