1186115-51-4

Basic information

• Product Name: 6-(1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER
• Synonyms: 6-(1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER;2-(1H-Pyrazol-1-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
• CAS NO: 1186115-51-4
• Molecular Formula: C14H18BN3O2
• Molecular Weight: 271.12262
• Mol File: 1186115-51-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-(1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1186115-51-4)
• EPA Substance Registry System: 6-(1H-PYRAZOL-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER(1186115-51-4)

Safety Data

• Hazardous Substances Data: 1186115-51-4(Hazardous Substances Data)

Usage

Description

6-(1H-Pyrazol-1-yl)pyridine-2-boronic acid pinacol ester is a chemical compound that belongs to the class of pyridine boronic acid esters. It is characterized by its unique structure and reactivity, which allows it to form stable complexes with a variety of transition-metal catalysts. This makes it a valuable reagent in organic synthesis and medicinal chemistry for the preparation of various pharmaceutical compounds.

Uses

Used in Organic Synthesis:
6-(1H-Pyrazol-1-yl)pyridine-2-boronic acid pinacol ester is used as a reagent in organic synthesis for the preparation of various pharmaceutical compounds. Its ability to form stable complexes with transition-metal catalysts makes it a versatile tool in the development of new drugs and materials.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-(1H-Pyrazol-1-yl)pyridine-2-boronic acid pinacol ester is used for the preparation of pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs and materials with potential therapeutic applications.
Used in Catalytic Cross-Coupling Reactions:
6-(1H-Pyrazol-1-yl)pyridine-2-boronic acid pinacol ester is utilized in catalytic cross-coupling reactions due to its ability to form stable complexes with transition-metal catalysts. This property makes it a valuable component in the synthesis of complex organic molecules and the development of advanced materials.