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Product Information

Product Name
Boc-O-methyl-L-tyrosine
Brand Name
Chem Impex
Product Number
01398
CAS
53267-93-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2762280
IUPAC Name
(2S)-3-(4-methoxyphenyl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
SLWWWZWJISHVOU-LBPRGKRZSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CC=C(C=C1)OC)C(=O)O

Application

Boc-O-methyl-L-tyrosine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require a protected amino acid. Its unique structure allows for selective reactions, making it easier to create complex peptide chains.

Drug Development: In pharmaceutical research, Boc-O-methyl-L-tyrosine is used to develop new drugs targeting neurological disorders. Its ability to mimic natural amino acids can enhance the efficacy of drug candidates.

Bioconjugation: The compound can be used in bioconjugation processes, where it helps attach therapeutic agents to proteins or antibodies, improving the specificity and effectiveness of treatments in targeted therapies.

Research in Neuroscience: This chemical is valuable in studies related to neurotransmitter synthesis, particularly in understanding the role of tyrosine derivatives in brain function and mood regulation.

Analytical Chemistry: Boc-O-methyl-L-tyrosine is utilized in analytical methods to assess the purity and composition of various compounds, providing researchers with reliable data for their studies.

References Data Source From Pubchem

19F- and 18F-arene deoxyfluorination via organic photoredox-catalysed polarity-reversed nucleophilic aromatic substitution

Publication Name: Nature Catalysis
Publication Date: 2020-08-24
DOI: 10.1038/s41929-020-0495-0

Design, synthesis, and in vitro antiplasmodial activity of 4-aminoquinolines containing modified amino acid conjugates

Publication Name: Medicinal Chemistry Research
Publication Date: 2016-03-25
DOI: 10.1007/s00044-016-1555-5