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Sku CI03777_25_G
Chem Impex
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Product Information

Product Name
Boc-L-trans-4-hydroxyproline
Brand Name
Chem Impex
Product Number
03777
CAS
13726-69-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
88804
IUPAC Name
(2S,4R)-4-hydroxy-1-(2-methylpropan-2-yl)oxycarbonylpyrrolidine-2-carboxylic acid
InChI Key
BENKAPCDIOILGV-RQJHMYQMSA-N
SMILES
CC(C)(C)OC(=O)N1CC@@H(CC@H1C(=O)O)O

Description

Boc-L-trans-4-hydroxyproline is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of bioactive peptides that can be used in pharmaceuticals.

Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their stability and bioavailability, which is crucial in medicinal chemistry.

Biomaterials: The compound is used in creating hydrogels and other biomaterials, which are essential in tissue engineering and regenerative medicine.

Research on Collagen: It plays a significant role in studying collagen stability and structure, providing insights into skin health and wound healing.

Cosmetic Formulations: Its properties make it beneficial in cosmetic products aimed at improving skin texture and hydration, appealing to the beauty and personal care industry.

References Data Source From Pubchem

Synthesis and Properties of 4-Amino-5-oxoproline Derivatives (A Review)

Publication Name: Russian Journal of General Chemistry
Publication Date: 2026-02-24
DOI: 10.1134/s1070363225606003

Precision in stereochemistry: the integral role of catalytic asymmetric Biginelli reaction in crafting enantiomerically pure dihydropyrimidinones

Publication Name: Molecular Diversity
Publication Date: 2024-03-27
DOI: 10.1007/s11030-024-10827-7

Copper-catalyzed C(sp)–H aryl amination enables modular synthesis of quinolines and 2-quinolinones

Publication Name: Science China Chemistry
Publication Date: 2023-10-23
DOI: 10.1007/s11426-023-1739-y

Chiral Polymer-Mediated Pd@MOF-808 for Efficient Sequential Asymmetric Reaction

Publication Name: Catalysis Letters
Publication Date: 2022-06-08
DOI: 10.1007/s10562-022-04053-9

Synthesis of Glecaprevir. Part 1

Publication Name: Synfacts
Publication Date: 2020-10-20
DOI: 10.1055/s-0040-1706322