$75.20

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI07023_1_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
4-tert-Butyl-L-phenylalanine
Brand Name
Chem Impex
Product Number
07023
CAS
82372-74-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2761795
IUPAC Name
(2S)-2-amino-3-(4-tert-butylphenyl)propanoic acid
InChI Key
CSJZKSXYLTYFPU-NSHDSACASA-N
SMILES
CC(C)(C)C1=CC=C(C=C1)CC@@H(C(=O)O)N

Application

4-tert-Butyl-L-phenylalanine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly in the development of peptide-based drugs, enhancing their efficacy and stability.

Protein Engineering: It is employed in the modification of proteins to improve their properties, such as solubility and thermal stability, making it valuable in biotechnology and enzyme engineering.

Research on Neurotransmitters: The compound is used in studies related to neurotransmitter activity, helping researchers understand its role in neurological functions and potential therapeutic applications.

Cosmetic Formulations: Its unique properties make it a candidate for use in cosmetic products, where it can enhance skin absorption and improve product performance.

Food Industry Applications: This compound can also be explored for flavor enhancement in food products, offering a potential advantage in creating more appealing taste profiles.

References Data Source From Pubchem

Genetically encoded amino acids with tert-butyl and trimethylsilyl groups for site-selective studies of proteins by NMR spectroscopy

Publication Name: Journal of Biomolecular NMR
Publication Date: 2017-12-02
DOI: 10.1007/s10858-017-0157-y

Design of substrate-based BCR-ABL kinase inhibitors using the cyclotide scaffold

Publication Name: Scientific Reports
Publication Date: 2015-08-12
DOI: 10.1038/srep12974

Neighbouring group processes in the deamination of protonated phenylalanine derivatives

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

Helical templating of oligopeptides by cyclodextrin dimers

Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2003-06-12
DOI: 10.1016/s0968-0896(03)00153-6