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Sku CI01386_250_G
Chem Impex
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Product Information

Product Name
Na-Boc-L-tryptophan
Brand Name
Chem Impex
Product Number
01386
CAS
13139-14-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
83169
IUPAC Name
(2S)-3-(1H-indol-3-yl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
NFVNYBJCJGKVQK-ZDUSSCGKSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CNC2=CC=CC=C21)C(=O)O

Description

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

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry where custom peptides are developed for therapeutic applications.

Drug Development: Its role in drug discovery is significant, as it helps in the design of compounds that can modulate biological pathways, particularly those involving serotonin receptors.

Biotechnology: In biotechnological applications, it is used in the production of recombinant proteins, enhancing the yield and stability of proteins during expression in various systems.

Research on Neurotransmitters: Researchers utilize it to study the metabolism and function of tryptophan in the brain, contributing to a better understanding of mood disorders and potential treatments.

Analytical Chemistry: It is employed in analytical methods to quantify tryptophan levels in biological samples, aiding in nutritional studies and health assessments.

References Data Source From Pubchem

New Benzoic Acid Derivatives as Potential Antimicrobial Drugs

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2025-08
DOI: 10.1007/s11094-025-03425-w

Discovery of New Cyclic Dipeptide from the Rare Actinobacterium Crossiella cryophilis CGMCC 4.1710

Publication Name: Chemistry of Natural Compounds
Publication Date: 2025-05
DOI: 10.1007/s10600-025-04691-6

Anamorelin

Publication Name: Pharmaceutical Substances
Publication Date: 2025

Improved automated one-pot two-step radiosynthesis of (S)-[18F]FETrp, a radiotracer for PET imaging of indoleamine 2,3-dioxygenase 1 (IDO1)

Publication Name: EJNMMI Radiopharmacy and Chemistry
Publication Date: 2024-04-02
DOI: 10.1186/s41181-024-00256-0

Cleavage of Photoremovable Groups

Publication Name: Science of Synthesis
Publication Date: 2024