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Sku CI06018_5_G
Chem Impex
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Product Information

Product Name
3-(1-Naphthyl)-DL-alanine
Brand Name
Chem Impex
Product Number
06018
CAS
28095-56-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
99505
IUPAC Name
2-amino-3-naphthalen-1-ylpropanoic acid
InChI Key
OFYAYGJCPXRNBL-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C=CC=C2CC(C(=O)O)N

Description

3-(1-Naphthyl)-DL-alanine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its structural similarity to neurotransmitters.

Biochemical Research: It is employed in studies investigating protein interactions and enzyme activity, helping researchers understand metabolic pathways and cellular functions.

Material Science: The compound is used in the development of novel materials, including polymers and coatings, which benefit from its unique chemical properties and stability.

Analytical Chemistry: It acts as a standard in chromatographic techniques, aiding in the accurate analysis of complex mixtures in various samples, including biological fluids.

Food Industry: This chemical is explored for its potential as a flavor enhancer or additive, providing a unique aromatic profile that can improve food products.

References Data Source From Pubchem

Theranostic PSMA ligands with optimized backbones for intraoperative multimodal imaging and photodynamic therapy of prostate cancer

Publication Name: European Journal of Nuclear Medicine and Molecular Imaging
Publication Date: 2022-01-14
DOI: 10.1007/s00259-022-05685-0

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

A Targeted Bivalent Androgen Receptor Binding Compound for Prostate Cancer Therapy

Publication Name: Hormones and Cancer
Publication Date: 2018-12-18
DOI: 10.1007/s12672-018-0353-6

Photoaffinity Labeling Methods to Explore Internalization Mechanisms of Arginine-Rich Cell-Penetrating Peptides

Publication Name: Photoaffinity Labeling for Structural Probing Within Protein
Publication Date: 2017
DOI: 10.1007/978-4-431-56569-7_11

Conformational transformation of ascidiacyclamide analogues induced by incorporating enantiomers of phenylalanine, 1-naphthylalanine or 2-naphthylalanine

Publication Name: Journal of peptide science : an official publication of the European Peptide Society
Publication Date: 2016-02-09
DOI: 10.1002/psc.2853