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Sku CI14332_5_G
Chem Impex
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Product Information

Product Name
Z-O-tert-butyl-L-tyrosine
Brand Name
Chem Impex
Product Number
14332
CAS
5545-54-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
978520
IUPAC Name
(2S)-3-4-(2-methylpropan-2-yl)oxyphenyl-2-(phenylmethoxycarbonylamino)propanoic acid
InChI Key
YKVBQSGNGCKQSV-SFHVURJKSA-N
SMILES
CC(C)(C)OC1=CC=C(C=C1)CC@@H(C(=O)O)NC(=O)OCC2=CC=CC=C2

Description

Z-O-tert-butyl-L-tyrosine is widely utilized in research focused on

Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing chemists to selectively modify amino acids without unwanted reactions.

Drug Development: It plays a crucial role in the design of pharmaceuticals, particularly in creating compounds that target specific proteins involved in diseases.

Biochemical Research: Researchers use it to study protein interactions and functions, providing insights into cellular processes and disease mechanisms.

Cosmetic Formulations: Due to its stability and compatibility, it is incorporated into skincare products to enhance the efficacy of active ingredients.

Food Industry: It can be used as a flavor enhancer or additive, improving the sensory qualities of food products while ensuring safety and compliance with regulations.

References Data Source From Pubchem

Peptide Bond Formation with the Aid of Coupling Reagents

Publication Name: The Practice of Peptide Synthesis
Publication Date: 1994
DOI: 10.1007/978-3-642-85055-4_11

Synthesis of a substituted fragment A17–21 of human insulin

Publication Name: Chemistry of Natural Compounds
Publication Date: 1979-09
DOI: 10.1007/bf00565965

Structure of the isomerization product of perfamine

Publication Name: Chemistry of Natural Compounds
Publication Date: 1979-09
DOI: 10.1007/bf00565964

Synthesis of protected peptides corresponding to fragment A13–16 of human insulin

Publication Name: Chemistry of Natural Compounds
Publication Date: 1979-07
DOI: 10.1007/bf00565074