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Product Information

Product Name
Boc-L-thiaproline
Brand Name
Chem Impex
Product Number
02735
CAS
51077-16-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
688405
IUPAC Name
(4R)-3-(2-methylpropan-2-yl)oxycarbonyl-1,3-thiazolidine-4-carboxylic acid
InChI Key
FJWNZTPXVSWUKF-LURJTMIESA-N
SMILES
CC(C)(C)OC(=O)N1CSCC@H1C(=O)O

Application

Boc-L-thiaproline 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 cyclic peptides that can enhance biological activity.

Drug Development: It plays a crucial role in medicinal chemistry, where it is used to design and synthesize novel drugs, especially those targeting specific receptors or enzymes.

Bioconjugation: Researchers leverage Boc-L-thiaproline for bioconjugation processes, allowing for the attachment of biomolecules to therapeutic agents, improving their efficacy and targeting capabilities.

Protein Engineering: Its unique structure aids in the modification of proteins, enabling scientists to create proteins with enhanced stability and functionality for various applications in biotechnology.

Research in Neuroscience: The compound is explored for its potential applications in neuroscience, particularly in studying the effects of modified peptides on neurological pathways and disorders.

References Data Source From Pubchem

New C(4)-esters of podophyllotoxin and epipodophyllotoxin with heterocyclic moieties

Publication Name: Russian Chemical Bulletin
Publication Date: 2023-09
DOI: 10.1007/s11172-023-4015-7

A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway

Publication Name: Journal of biomolecular screening
Publication Date: 2016-07
DOI: 10.1177/1087057116635503

Identification of tetrameric opioid peptides from a combinatorial library composed of L-, D- and non-proteinogenic amino acids

Publication Name: Peptides 1994
Publication Date: 1995
DOI: 10.1007/978-94-011-1468-4_370