$418.40

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. No lead time available. Please request a quote.
Sku CI00685_100_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
Boc-O-2-bromo-Z-L-tyrosine
Brand Name
Chem Impex
Product Number
00685
CAS
47689-67-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
12898155
IUPAC Name
(2S)-3-4-(2-bromophenyl)methoxycarbonyloxyphenyl-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
UYWMYJQSTUVRHR-SFHVURJKSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CC=C(C=C1)OC(=O)OCC2=CC=CC=C2Br)C(=O)O

Application

Boc-O-2-bromo-Z-L-tyrosine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex proteins for various studies, including drug development and biomolecular research.

Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their efficacy and specificity. This is particularly valuable in the pharmaceutical industry where targeted therapies are essential.

Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to therapeutic agents. This application is crucial in developing antibody-drug conjugates, which improve the delivery of drugs to specific cells.

Research in Neuroscience: Boc-O-2-bromo-Z-L-tyrosine can be utilized in studies related to neurotransmitter activity, aiding researchers in understanding the role of tyrosine derivatives in brain function and disorders.

Analytical Chemistry: It is employed in analytical methods to quantify and analyze tyrosine derivatives in biological samples, providing insights into metabolic pathways and disease states.

References Data Source From Pubchem

Boc/Bzl Solid-Phase Synthesis of Deltorphin II and Its Analogs without the Utilization of Anhydrous Hydrogen Fluoride

Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2024-10
DOI: 10.1134/s1068162024050297

Synthesis and Structure-Activity Relationship of [Nle10]Neurokinin A (4–10) Analogs with Constraint in the Backbone and at Position Six

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2007-03-10
DOI: 10.1007/s10989-007-9087-y

Heterogeneous catalytic transfer hydrogenation in peptide synthesis

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2002-07
DOI: 10.1007/bf02538377|10.1023/a:1024178830961