1310405-03-8

Basic information

• Product Name: 6-(4-METHYL-1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER
• Synonyms: 6-(4-METHYL-1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER;2-(4-Methyl-1H-pyrazol-1-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
• CAS NO: 1310405-03-8
• Molecular Formula: C15H20BN3O2
• Molecular Weight: 285.1492
• Mol File: 1310405-03-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-(4-METHYL-1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(4-METHYL-1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1310405-03-8)
• EPA Substance Registry System: 6-(4-METHYL-1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1310405-03-8)

Safety Data

• Hazardous Substances Data: 1310405-03-8(Hazardous Substances Data)

Usage

General Description

6-(4-methyl-1H-pyrazol-1-yl)pyridine-2-boronic acid pinacol ester is a chemical compound with a boronic acid functional group, often used in the field of organic chemistry as a reagent and intermediate in the synthesis of various other compounds. It is commonly utilized as a building block in the production of pharmaceuticals, agrochemicals, and materials science applications. The compound possesses the potential for cross-coupling reactions and is a valuable tool in the development of new drugs and materials due to its ability to form stable covalent bonds with other molecules and excellent regioselectivity. Additionally, it can also be employed in the construction of functionalized heterocyclic compounds and has promising applications in the development of novel biologically active molecules.