$200.90

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. Please allow 4-6 weeks for production.
Sku CI02854_25_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
L-3,4-Dichlorophenylalanine
Brand Name
Chem Impex
Product Number
02854
CAS
52794-99-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2761498
IUPAC Name
(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid
InChI Key
NRCSJHVDTAAISV-QMMMGPOBSA-N
SMILES
C1=CC(=C(C=C1CC@@H(C(=O)O)N)Cl)Cl

Application

L-3,4-Dichlorophenylalanine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy.

Neurotransmitter Research: It is employed in studies investigating neurotransmitter systems, especially in understanding the role of amino acids in brain function, which can lead to breakthroughs in treating mental health conditions.

Biochemical Assays: L-3,4-Dichlorophenylalanine is used in enzyme inhibition assays, helping researchers evaluate the activity of specific enzymes, which is crucial in drug discovery and development.

Protein Engineering: The compound is applied in the modification of proteins to study structure-function relationships, enabling advancements in biotechnology and therapeutic protein design.

Amino Acid Research: It is significant in the study of amino acid metabolism and its implications in various diseases, providing insights that could lead to novel treatment strategies.

References Data Source From Pubchem

Discovery of non-proteinogenic amino acids inhibiting biofilm formation by S. aureus and methicillin-resistant S. aureus

Publication Name: Bioorganic & Medicinal Chemistry Letters
Publication Date: 2021-09-15
DOI: 10.1016/j.bmcl.2021.128259

Neighbouring group processes in the deamination of protonated phenylalanine derivatives

Publication Name: Organic & Biomolecular Chemistry
Publication Date: 2005-10-21
DOI: 10.1039/b503355a

Characterization of antinociceptive activity of novel endomorphin-2 and morphiceptin analogs modified in the third position

Publication Name: Biochemical Pharmacology
Publication Date: 2005-01-01
DOI: 10.1016/j.bcp.2004.09.011

Structure Elucidation of Peptides with Unnatural Amino Acids Using an Automated Protein Sequencer

Publication Name: Peptides: The Wave of the Future
Publication Date: 2001
DOI: 10.1007/978-94-010-0464-0_136