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Product Information

Product Name
Boc-O-benzyl-D-serine
Brand Name
Chem Impex
Product Number
01550
CAS
47173-80-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2733693
IUPAC Name
(2R)-2-(2-methylpropan-2-yl)oxycarbonylamino-3-phenylmethoxypropanoic acid
InChI Key
DMBKPDOAQVGTST-GFCCVEGCSA-N
SMILES
CC(C)(C)OC(=O)NC@H(COCC1=CC=CC=C1)C(=O)O

Application

Boc-O-benzyl-D-serine is widely utilized in research focused on:

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

Drug Development: It plays a role in the development of novel therapeutic agents, particularly in designing inhibitors for various biological targets, enhancing the efficacy of drug candidates.

Biochemical Research: Researchers use it to study enzyme mechanisms and protein interactions, providing insights into cellular processes and potential drug targets.

Material Science: The compound is utilized in creating bio-compatible materials for medical applications, such as drug delivery systems, due to its favorable properties.

Analytical Chemistry: Boc-O-benzyl-D-serine is employed in chromatography and mass spectrometry as a standard for analyzing amino acids and peptides, ensuring accurate results in research and quality control.

References Data Source From Pubchem

Synthesis of Erythrochelin: A Hydroxamate-Type Siderophore from Saccharopolyspora erythraea

Publication Name: Synthesis
Publication Date: 2016-08-24
DOI: 10.1055/s-0035-1560564

Synthesis of BMS-317180

Publication Name: Synfacts
Publication Date: 2009-09-22
DOI: 10.1055/s-0029-1217858

Total Synthesis of Arylomycin A2, a Signal Peptidase I (SPase I) Inhibitor

Publication Name: Synlett
Publication Date: 2008-08-22
DOI: 10.1055/s-2008-1078209