1204112-62-8

Basic information

• Product Name: 2-aMinopyridin-3-ylboronic acid
• Synonyms: 2-aMinopyridin-3-ylboronic acid;2-AMINOPYRIDIN-3-YLBORONIC ACID HCl;2-AMinopyridine-3-boronic acid
• CAS NO: 1204112-62-8
• Molecular Formula: C5H7BN2O2
• Molecular Weight: 137.93228
• Mol File: 1204112-62-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 379.3±52.0 °C(Predicted)
• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.30±0.53(Predicted)
• CAS DataBase Reference: 2-aMinopyridin-3-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-aMinopyridin-3-ylboronic acid(1204112-62-8)
• EPA Substance Registry System: 2-aMinopyridin-3-ylboronic acid(1204112-62-8)

Safety Data

• Hazardous Substances Data: 1204112-62-8(Hazardous Substances Data)

Usage

General Description

2-Aminopyridin-3-ylboronic acid, also known as APYB, is a chemical compound that belongs to the class of boronic acids. It is commonly used in organic synthesis as a reagent for the Suzuki coupling reaction, which is a popular method for forming carbon-carbon bonds. APYB is an important component in the production of pharmaceuticals and agrochemicals, as it serves as a key building block for creating complex molecular structures. Its unique properties make it a valuable tool in the field of chemical research and development, with potential applications in the synthesis of diverse organic molecules. Additionally, APYB can be used as a ligand in transition metal-catalyzed reactions, further extending its utility in various chemical processes.

Downstream Products

• 1258934-83-6 tert-butyl N-{2-(2-aminopyridin-3-yl)-5-[2-(4-fluorophenyl)ethynyl]-1,3-thiazol-4-yl}carbamate