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Product Information

Product Name
Boc-(4-aminomethyl) benzoic acid
Brand Name
Chem Impex
Product Number
07119
CAS
33233-67-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
853605
IUPAC Name
4-(2-methylpropan-2-yl)oxycarbonylaminomethylbenzoic acid
InChI Key
LNKHBRDWRIIROP-UHFFFAOYSA-N
SMILES
CC(C)(C)OC(=O)NCC1=CC=C(C=C1)C(=O)O

Application

Boc-(4-aminomethyl) benzoic acid is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing yield. Its stability under various conditions makes it a preferred choice for chemists.

Drug Development: In pharmaceutical research, it is used to modify drug candidates, improving their solubility and bioavailability. This can lead to more effective treatments with fewer side effects.

Bioconjugation: The compound is employed in bioconjugation processes, linking biomolecules to create targeted therapies. This is particularly beneficial in developing personalized medicine approaches.

Material Science: It finds applications in creating functionalized polymers and materials, enhancing properties like thermal stability and mechanical strength, which are crucial in various industrial applications.

Analytical Chemistry: Boc-(4-aminomethyl) benzoic acid is used as a standard in analytical methods, aiding in the quantification of related compounds in complex mixtures, thereby improving accuracy in research findings.

References Data Source From Pubchem

Propylphosphonic Anhydride (T3P®)-Mediated One-Pot Rearrangement of Carboxylic Acids to Carbamates

Publication Name: Synthesis
Publication Date: 2011-03-22
DOI: 10.1055/s-0030-1259964

Covalent Tethering of Organic Functionality to the Surface of Glassy Carbon Electrodes by Using Electrochemical and Solid‐Phase Synthesis Methodologies

Publication Name: Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Date: 2008-02-28
DOI: 10.1002/chem.200701559

Semisynthetic preparation of leucomycin derivatives: Introduction of aromatic side chains by reductive amination

Publication Name: Molecular Diversity
Publication Date: 2005-01
DOI: 10.1007/s11030-005-1304-z