Product Added to Cart!
$316.30

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI12100_100_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
L-Proline ethyl ester hydrochloride
Brand Name
Chem Impex
Product Number
12100
CAS
33305-75-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11679912
IUPAC Name
ethyl (2S)-pyrrolidine-2-carboxylate;hydrochloride
InChI Key
DUJGQVVONTYHLT-RGMNGODLSA-N
SMILES
CCOC(=O)C@@H1CCCN1.Cl

Description

L-Proline ethyl ester hydrochloride 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 pharmaceutical industry, where it can enhance the stability and bioactivity of peptide drugs.

Chiral Auxiliary: It acts as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds, which are crucial in drug development.

Biochemical Research: Researchers use it to study protein folding and stability, providing insights into enzyme mechanisms and potential therapeutic targets.

Food Industry: It can be applied in the formulation of flavor enhancers and food additives, improving the taste profile of various products.

Cosmetic Formulations: The compound is also incorporated into cosmetic products for its moisturizing properties, contributing to skin hydration and overall product efficacy.

References Data Source From Pubchem

Developing the Optimal Synthetic Schem for the Potential Nootropic Drug GZK-111, N-Phenylacetylglycyl-L-Proline Ethyl Ester

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2020-09-28
DOI: 10.1007/s11094-020-02251-6

N-Phenylacetylglycyl-L-Proline Ethyl Ester Converts into Cyclo-L-Prolylglycine Showing a Similar Spectrum of Neuropsychotropic Activity

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2017-02-17
DOI: 10.1007/s11094-017-1516-4

Synthesis and anticancer activities of novel (tetrahydrobenzo [4,5] thieno [2,3-d] pyrimidine-4-yl)-pyrolidine-2-carboxylic acid derivatives

Publication Name: Medicinal Chemistry Research
Publication Date: 2016-08-03
DOI: 10.1007/s00044-016-1692-x

Synthesis and nootropic activity of pyrrolidino[1,2-a]diazacycloalkanes

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 1996-09-01
DOI: 10.1007/bf02219346