$270.10

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI15884_250_MG
Chem Impex
Get Bulk Quote

Product Information

Product Name
Boc-(R)-a-allylproline
Brand Name
Chem Impex
Product Number
15884
CAS
144085-23-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2761958
IUPAC Name
(2R)-1-(2-methylpropan-2-yl)oxycarbonyl-2-prop-2-enylpyrrolidine-2-carboxylic acid
InChI Key
ZTMLHNDSVVOEEH-ZDUSSCGKSA-N
SMILES
CC(C)(C)OC(=O)N1CCCC@@1(CC=C)C(=O)O

Application

Boc-(R)-a-allylproline is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in creating cyclic peptides that can have enhanced biological activity.

Drug Development: Its unique structure allows for the design of novel pharmaceuticals, especially in the development of drugs targeting neurological disorders, due to its ability to mimic natural amino acids.

Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.

Research in Organocatalysis: Boc-(R)-a-allylproline is employed as an organocatalyst in various organic reactions, providing an environmentally friendly alternative to traditional metal catalysts.

Studying Protein Interactions: It is used in research to investigate protein-ligand interactions, helping scientists understand how proteins function and how they can be targeted for therapeutic purposes.

References Data Source From Pubchem

Cycloaddition Initiated by Ynolates: High-Energy Dianion Equivalents as a Molecular Glue

Publication Name: Synlett
Publication Date: 2021-11-22
DOI: 10.1055/s-0040-1719857

Diversity-Oriented Asymmetric Synthesis

Publication Name: Synthesis
Publication Date: 2014-07-30
DOI: 10.1055/s-0033-1341247