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Chem Impex
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Product Information

Product Name
2-Bromo-L-phenylalanine
Brand Name
Chem Impex
Product Number
07428
CAS
42538-40-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
193338
IUPAC Name
(2S)-2-amino-3-(2-bromophenyl)propanoic acid
InChI Key
JFVLNTLXEZDFHW-QMMMGPOBSA-N
SMILES
C1=CC=C(C(=C1)CC@@H(C(=O)O)N)Br

Application

2-Bromo-L-phenylalanine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a valuable building block in the synthesis of novel pharmaceuticals, particularly in the development of drugs targeting neurological disorders.

Protein Engineering: It is used as a non-canonical amino acid in protein engineering, allowing researchers to study protein structure and function with enhanced specificity.

Biochemical Research: The compound is employed in studies of enzyme activity and inhibition, helping scientists understand metabolic pathways and develop potential inhibitors for therapeutic use.

Neuroscience Studies: Its application in neuroscience research aids in the investigation of neurotransmitter systems, providing insights into conditions such as depression and anxiety.

Labeling and Imaging: 2-Bromo-L-phenylalanine can be used in labeling techniques for imaging studies, allowing for better visualization of biological processes in live cells.

References Data Source From Pubchem

Lobetyolin, an anti-AD factor from the diet campanulaceae source, metabolism regulation and target exploration

Publication Name: Natural Products and Bioprospecting
Publication Date: 2025-09-12
DOI: 10.1007/s13659-025-00549-0

Rationally introducing non-canonical amino acids to enhance catalytic activity of LmrR for Henry reaction

Publication Name: Bioresources and Bioprocessing
Publication Date: 2024-02-29
DOI: 10.1186/s40643-024-00744-w

Recent advancements in enzyme engineering via site-specific incorporation of unnatural amino acids

Publication Name: World Journal of Microbiology and Biotechnology
Publication Date: 2021-11-06
DOI: 10.1007/s11274-021-03177-1

Improving the N-terminal diversity of sansanmycin through mutasynthesis

Publication Name: Microbial Cell Factories
Publication Date: 2016-05-06
DOI: 10.1186/s12934-016-0471-1

Optimization by Experimental Design of Precursor Synthesis and Radiolabeling of 2-Iodo-L-Phenylalanine, a Novel Amino Acid for Tumor Imaging

Publication Name: Cancer Biotherapy and Radiopharmaceuticals
Publication Date: 2006-06
DOI: 10.1089/cbr.2006.21.235