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Product Information

Product Name
Boc-O-benzyl-L-threonine
Brand Name
Chem Impex
Product Number
00440
CAS
15260-10-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
1549483
IUPAC Name
(2S,3R)-2-(2-methylpropan-2-yl)oxycarbonylamino-3-phenylmethoxybutanoic acid
InChI Key
CTXPLTPDOISPTE-YPMHNXCESA-N
SMILES
CC@H(C@@H(C(=O)O)NC(=O)OC(C)(C)C)OCC1=CC=CC=C1

Application

Boc-O-benzyl-L-threonine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.

Drug Development: Its unique properties make it an important intermediate in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways.

Biotechnology: In the field of biotechnology, it is used to modify proteins, enhancing their stability and activity, which is crucial for therapeutic applications.

Research in Enzyme Inhibition: Scientists utilize this compound to study enzyme interactions, providing insights into metabolic pathways and potential drug targets.

Analytical Chemistry: It is employed in various analytical techniques, helping to identify and quantify other compounds in complex mixtures, which is essential for quality control in manufacturing.

References Data Source From Pubchem

Synthesis of P- and S-Stereogenic Compounds via Enantioselective C–H Functionalization

Publication Name: Synthesis
Publication Date: 2022-05-12
DOI: 10.1055/a-1802-6793

In Situ Neutralization Protocols for Boc-SPPS

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2020
DOI: 10.1007/978-1-0716-0227-0_3

Synthesis of the C-Terminal Macrocycle of Asperipin-2a

Publication Name: Synfacts
Publication Date: 2019-05-20
DOI: 10.1055/s-0037-1612530

Heterogeneous Catalysis

Publication Name: Science of Synthesis
Publication Date: 2017

The best and the brightest: exploiting tryptophan-sensitized Tb(3+) luminescence to engineer lanthanide-binding tags

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2015
DOI: 10.1007/978-1-4939-2020-4_14