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Chem Impex
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Product Information

Product Name
O-Benzyl-D-serine
Brand Name
Chem Impex
Product Number
03313
CAS
10433-52-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
112114
IUPAC Name
(2R)-2-amino-3-phenylmethoxypropanoic acid
InChI Key
IDGQXGPQOGUGIX-SECBINFHSA-N
SMILES
C1=CC=C(C=C1)COCC@H(C(=O)O)N

Description

O-Benzyl-D-serine is widely utilized in research focused on

Pharmaceutical Development: This compound serves as a valuable building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.

Biochemical Research: It is employed in studies investigating the role of amino acids in protein synthesis and enzyme activity, providing insights into metabolic pathways.

Neuroscience Applications: O-Benzyl-D-serine is used to explore neurotransmitter interactions, aiding researchers in understanding synaptic transmission and potential treatments for mental health conditions.

Peptide Synthesis: The compound is integral in the synthesis of peptides, which are crucial for developing therapeutic agents and understanding protein structure-function relationships.

Analytical Chemistry: It is utilized as a standard in analytical methods, helping to ensure the accuracy and reliability of results in various chemical analyses.

References Data Source From Pubchem

An untargeted metabolomics approach to study changes of the medium during human cornea culture

Publication Name: Metabolomics : Official journal of the Metabolomic Society
Publication Date: 2024-04-06
DOI: 10.1007/s11306-024-02102-5

Bioactivity Focus of α-Cyano-4-hydroxycinnamic acid (CHCA) Leads to Effective Multifunctional Aldose Reductase Inhibitors

Publication Name: Scientific Reports
Publication Date: 2016-04-25
DOI: 10.1038/srep24942

Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand-Exchange

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2013
DOI: 10.1007/978-1-62703-263-6_11

hydantoin racemase 5.1.99.5

Publication Name: Class 3.4–6 Hydrolases, Lyases, Isomerases, Ligases
Publication Date: 2013
DOI: 10.1007/978-3-642-36260-6_77

Chiral recognition of aromatic compounds by beta-cyclodextrin based on bimodal complexation

Publication Name: Journal of Molecular Modeling
Publication Date: 2005-05-18
DOI: 10.1007/s00894-004-0233-6