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Chem Impex
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Product Information

Product Name
Z-L-trans-4-hydroxyproline methyl ester
Brand Name
Chem Impex
Product Number
06503
CAS
64187-48-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
688411
IUPAC Name
1-O-benzyl 2-O-methyl (2S,4R)-4-hydroxypyrrolidine-1,2-dicarboxylate
InChI Key
VVKAGQHUUDRPOI-NEPJUHHUSA-N
SMILES
COC(=O)C@@H1CC@H(CN1C(=O)OCC2=CC=CC=C2)O

Application

Z-L-trans-4-hydroxyproline methyl ester is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a valuable intermediate in synthesizing various pharmaceuticals, particularly those targeting collagen-related disorders, enhancing drug efficacy and specificity.

Biochemical Research: It is employed in studies examining protein folding and stability, providing insights into the structural biology of proteins, which is crucial for drug design and development.

Cosmetic Formulations: The compound is incorporated into skincare products for its moisturizing properties, helping to improve skin texture and hydration, making it a popular choice in the cosmetic industry.

Food Industry: It is used as a food additive to enhance the nutritional profile of certain products, particularly in functional foods aimed at improving health benefits.

Material Science: Z-L-trans-4-hydroxyproline methyl ester is explored in the development of biodegradable polymers, contributing to sustainable materials that reduce environmental impact.

References Data Source From Pubchem

Hindered Dialkyl Ether Synthesis Electrified

Publication Name: Synfacts
Publication Date: 2019-12-13
DOI: 10.1055/s-0039-1691380

Synthesis of Vaniprevir (MK-7009)

Publication Name: Synfacts
Publication Date: 2011-12-19
DOI: 10.1055/s-0031-1289913

Synthesis of β-galactosyl-(hydroxy amino acid) derivatives using β-galactosidase activity ofAchatina achatina digestive juice

Publication Name: Biotechnology Letters
Publication Date: 1994-07
DOI: 10.1007/bf00136470