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Sku CI05320_100_G
Chem Impex
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Product Information

Product Name
N,O-Bis-Boc-L-tyrosine
Brand Name
Chem Impex
Product Number
05320
CAS
20866-48-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7010630
IUPAC Name
(2S)-2-(2-methylpropan-2-yl)oxycarbonylamino-3-4-(2-methylpropan-2-yl)oxycarbonyloxyphenylpropanoic acid
InChI Key
MRYIHKCPPKHOPJ-AWEZNQCLSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CC=C(C=C1)OC(=O)OC(C)(C)C)C(=O)O

Description

N,O-Bis-Boc-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 in solid-phase peptide synthesis, enhancing the efficiency and yield of the process.

Drug Development: It plays a crucial role in the development of pharmaceuticals, especially in creating prodrugs that improve the bioavailability of therapeutic agents.

Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics.

Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is employed in studies exploring the mechanisms of action in neuropharmacology, aiding in the understanding of brain functions.

Cosmetic Formulations: Its properties make it suitable for use in cosmetic products, where it can enhance skin hydration and provide antioxidant benefits, appealing to the beauty industry.

References Data Source From Pubchem

Reductive Radical Cyclization of Tyrosine and Phenylalanine with Alkenes

Publication Name: Synfacts
Publication Date: 2019-08-20
DOI: 10.1055/s-0039-1690515

Synthesis and reactivity of the monosaccharide esters of amino acids as models of teichoic acid fragment

Publication Name: Glycoconjugate Journal
Publication Date: 2000-05
DOI: 10.1023/a:1007157018792

tert-Butoxycarbonylation of tyrosine and other phenolic amino acids with di-tert-butyl pyrocarbonate

Publication Name: Chemistry of Natural Compounds
Publication Date: 1982-01
DOI: 10.1007/bf00581621