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Sku CI05319_1_G
Chem Impex
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Product Information

Product Name
Na-Boc-L-tryptophan methyl ester
Brand Name
Chem Impex
Product Number
05319
CAS
33900-28-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7021503
IUPAC Name
methyl (2S)-3-(1H-indol-3-yl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoate
InChI Key
QXLOVPXUZAOKBL-AWEZNQCLSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CNC2=CC=CC=C21)C(=O)OC

Description

Na-Boc-L-tryptophan methyl ester is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require tryptophan residues, enhancing the development of new therapeutic agents.

Drug Development: Its unique structure allows for modifications that can improve the bioavailability and efficacy of pharmaceuticals, making it valuable in the pharmaceutical industry.

Biochemical Research: Researchers use it to study protein interactions and enzyme activities, providing insights into metabolic pathways and potential drug targets.

Cosmetic Formulations: The compound's properties can be leveraged in the formulation of skincare products, offering benefits like improved skin hydration and anti-aging effects.

Food Industry: It can be used as a flavoring agent or nutritional supplement, capitalizing on its amino acid profile to enhance food products.

References Data Source From Pubchem

Tryptophan N 1-Alkylation: Quick and Simple Access to Diversely Substituted Tryptophans

Publication Name: Synthesis
Publication Date: 2021-03-16
DOI: 10.1055/a-1404-5079

Intramolecular Diels–Alder Reactions of Oxazoles, Imidazoles, and Thiazoles

Publication Name: Synthesis
Publication Date: 2020-12-14
DOI: 10.1055/s-0040-1705991

Modification of Tryptophan by Using Triarylbismuthines and Copper(II) Acetate

Publication Name: Synfacts
Publication Date: 2020-10-20
DOI: 10.1055/s-0040-1706524

Synthesis of α-Amanitin

Publication Name: Synfacts
Publication Date: 2018-05-17
DOI: 10.1055/s-0037-1609851

Synthetic Access to 3,5,7-Trisubstituted Indoles Enabled by Iridium­-Catalyzed C–H Borylation

Publication Name: Synthesis
Publication Date: 2017-05-08
DOI: 10.1055/s-0036-1589018