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Product Information

Product Name
Boc-L-phenylalanine
Brand Name
Chem Impex
Product Number
00775
CAS
13734-34-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
77857
IUPAC Name
(2S)-2-(2-methylpropan-2-yl)oxycarbonylamino-3-phenylpropanoic acid
InChI Key
ZYJPUMXJBDHSIF-NSHDSACASA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CC=CC=C1)C(=O)O

Application

Boc-L-phenylalanine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.

Drug Development: In pharmaceuticals, Boc-L-phenylalanine is used to create peptide-based drugs. Its incorporation can enhance the bioactivity and stability of therapeutic peptides, making them more effective in treating diseases.

Biotechnology: Researchers in biotechnology utilize this compound for the production of modified proteins. By incorporating Boc-L-phenylalanine, scientists can study protein interactions and functions more effectively.

Analytical Chemistry: It is employed in various analytical techniques, including chromatography, to separate and identify amino acids and peptides. This application is crucial for quality control in food and pharmaceutical industries.

Research in Neuroscience: The compound is used in studies related to neurotransmitter synthesis, particularly in understanding the role of phenylalanine in brain function and its implications in disorders like phenylketonuria.

References Data Source From Pubchem

Synthesis and Properties of 4-Amino-5-oxoproline Derivatives (A Review)

Publication Name: Russian Journal of General Chemistry
Publication Date: 2026-02-24
DOI: 10.1134/s1070363225606003

Reduction of Alkyl- and Alkoxybenzenes

Publication Name: Science of Synthesis
Publication Date: 2026

Synthesis and Properties of Carboxonium-Substituted Derivatives of the Octahydrotriborate Anion

Publication Name: Russian Journal of Inorganic Chemistry
Publication Date: 2025-12
DOI: 10.1134/s0036023625603666

In-vitro and in-silico screening of amino acid based-cholesteryl esters: comparative investigation to explore possible triple-negative breast cancer targets

Publication Name: Future Journal of Pharmaceutical Sciences
Publication Date: 2025-11-12
DOI: 10.1186/s43094-025-00903-6

A Photolabile Backbone Amide Linker for the Solid-Phase Synthesis of Cyclic Peptides and C-terminal Thioesters

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2025-09-08
DOI: 10.1007/s10989-025-10752-9