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Product Information

Product Name
Boc-D-tyrosine
Brand Name
Chem Impex
Product Number
02896
CAS
70642-86-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
1549481
IUPAC Name
(2R)-3-(4-hydroxyphenyl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
CNBUSIJNWNXLQQ-LLVKDONJSA-N
SMILES
CC(C)(C)OC(=O)NC@H(CC1=CC=C(C=C1)O)C(=O)O

Application

Boc-D-tyrosine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is particularly beneficial in pharmaceutical research where precise modifications are crucial.

Drug Development: Boc-D-tyrosine is often used in the development of novel therapeutic agents, especially in creating compounds that target specific biological pathways. Its ability to enhance solubility can improve the bioavailability of drugs.

Bioconjugation: In bioconjugation applications, Boc-D-tyrosine can be utilized to link biomolecules, such as proteins and antibodies, to drug molecules, enhancing their therapeutic efficacy and targeting capabilities.

Research in Neuroscience: This compound is important in studies related to neurotransmitter systems, particularly in understanding the role of tyrosine derivatives in brain function and mental health.

Cosmetic Formulations: Due to its properties, Boc-D-tyrosine is also explored in cosmetic chemistry for formulating products that promote skin health, leveraging its antioxidant potential.

References Data Source From Pubchem

A Rapid and Highly Diastereoselective Synthesis of Enantiomerically Pure (4R,5R)- and (4S,5S)-Isocytoxazone

Publication Name: Synlett
Publication Date: 2011-05-13
DOI: 10.1055/s-0030-1260561

Chiral effects of alkyl-substituted derivatives of N,O-bismethacryloyl ethanolamine on the performance of one monomer molecularly imprinted polymers (OMNiMIPs)

Publication Name: Analytical and Bioanalytical Chemistry
Publication Date: 2007-06-13
DOI: 10.1007/s00216-007-1364-2

An Effective Route to (-)-Aphanorphine Using d-Tyrosine as a Chiral Building Block

Publication Name: Synthesis
Publication Date: 2007-01
DOI: 10.1055/s-2006-958931

A recombinant human stromelysin catalytic domain identifying tryptophan derivatives as human stromelysin inhibitors

Publication Name: Journal of Medicinal Chemistry
Publication Date: 1994-01-07
DOI: 10.1021/jm00027a027