1598387-84-8

Basic information

• Product Name: 3-Fluoro-2-methoxypyridine-4-boronic acid
• Synonyms: 3-Fluoro-2-methoxypyridine-4-boronic acid
• CAS NO: 1598387-84-8
• Molecular Formula: C6H7BFNO3
• Molecular Weight: 170.9340832
• Mol File: 1598387-84-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 317.1±52.0 °C(Predicted)
• Appearance: /
• Density: 1.34±0.1 g/cm3(Predicted)
• PKA: 6.91±0.58(Predicted)
• CAS DataBase Reference: 3-Fluoro-2-methoxypyridine-4-boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Fluoro-2-methoxypyridine-4-boronic acid(1598387-84-8)
• EPA Substance Registry System: 3-Fluoro-2-methoxypyridine-4-boronic acid(1598387-84-8)

Safety Data

• Hazardous Substances Data: 1598387-84-8(Hazardous Substances Data)

Usage

Description

3-Fluoro-2-methoxypyridine-4-boronic acid is an organic compound characterized by the chemical formula C6H6BFO3N. It is a derivative of boronic acid, featuring a pyridine ring with a fluorine atom and a methoxy group at the 3and 2-positions, respectively. 3-Fluoro-2-methoxypyridine-4-boronic acid is recognized for its role in organic synthesis, particularly in the creation of pharmaceuticals, agrochemicals, and materials due to its versatile reactivity and solubility.

Uses

Used in Pharmaceutical Synthesis:
3-Fluoro-2-methoxypyridine-4-boronic acid is utilized as a key building block in the synthesis of pharmaceuticals. Its boronic acid functional group facilitates Suzuki coupling reactions, which are pivotal for the formation of carbon-carbon bonds, thereby enabling the construction of complex molecular structures with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 3-Fluoro-2-methoxypyridine-4-boronic acid serves as an intermediate for the development of new compounds with pesticidal properties. The ability of this compound to engage in cross-coupling reactions allows for the creation of a diverse range of agrochemicals designed to protect crops from pests and diseases.
Used in Material Science:
3-Fluoro-2-methoxypyridine-4-boronic acid is also employed in material science as a component in the synthesis of advanced materials. The presence of the fluorine and methoxy substituents on the pyridine ring can modulate the compound's properties, such as reactivity and solubility, making it suitable for the development of materials with specific characteristics for various applications.
Organic Synthesis:
3-Fluoro-2-methoxypyridine-4-boronic acid is used as a versatile reagent in organic synthesis for its ability to participate in a variety of chemical reactions, including but not limited to Suzuki coupling, which is crucial for the formation of carbon-carbon bonds and the synthesis of complex organic molecules.