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Sku CI00429_25_G
Chem Impex
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Product Information

Product Name
O-tert-Butyl-L-serine
Brand Name
Chem Impex
Product Number
00429
CAS
18822-58-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7004940
IUPAC Name
(2S)-2-amino-3-(2-methylpropan-2-yl)oxypropanoic acid
InChI Key
DDCPKNYKNWXULB-YFKPBYRVSA-N
SMILES
CC(C)(C)OCC@@H(C(=O)O)N

Application

O-tert-Butyl-L-serine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of pharmaceuticals and biologically active compounds.

Protein Engineering: It is employed in the modification of proteins to enhance their stability and activity, making it crucial for biotechnological applications.

Drug Development: Researchers use O-tert-Butyl-L-serine in the design of new drugs, especially in the field of cancer therapy, due to its ability to influence molecular interactions.

Biochemical Research: This chemical is important in studying enzyme mechanisms and protein-ligand interactions, providing insights that can lead to innovative therapeutic strategies.

Cosmetic Formulations: Its properties make it suitable for use in cosmetic products, where it can enhance skin hydration and improve product stability.

References Data Source From Pubchem

Design and Evaluation of ATN-161 Analogues as Fusion Inhibitors Targeting Integrins in SARS-CoV-2

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2025-05-30
DOI: 10.1007/s10989-025-10734-x

Incorporation of Azide and Alkyne Functionalities into Peptides

Publication Name: Science of Synthesis
Publication Date: 2021

QSPR modeling of optical rotation of amino acids using specific quantum chemical descriptors

Publication Name: Journal of Molecular Modeling
Publication Date: 2018-02-17
DOI: 10.1007/s00894-018-3593-z

O-Phosphoserine sulfhydrylase

Publication Name: Class 2 Transferases
Publication Date: 2009
DOI: 10.1007/978-3-540-85697-9_39