168267-41-2 | 3,4-Difluorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$22.00	$16.00
100g	98%	in stock	$56.00	$39.00
500g	98%	in stock	$253.00	$177.00

Description

• Catalog Number: AA90466
• Chemical Name: 3,4-Difluorophenylboronic acid
• CAS Number: 168267-41-2
• Molecular Formula: C6H5BF2O2
• Molecular Weight: 157.9105
• MDL Number: MFCD00807405
• SMILES: OB(c1ccc(c(c1)F)F)O

Computed Properties

• Complexity: 134
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

3,4-Difluorobenzeneboronic Acid is a versatile chemical compound that finds wide application in chemical synthesis. As a boronic acid derivative, it is commonly used as a key building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure containing fluorine atoms imparts distinct properties that are highly valuable in organic synthesis.One of the primary applications of 3,4-Difluorobenzeneboronic Acid is in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method allows for the selective formation of carbon-carbon bonds, enabling the rapid construction of complex molecular structures. By incorporating this boronic acid into the reaction, chemists can achieve precise control over the coupling process, leading to high yields of the desired products.Furthermore, 3,4-Difluorobenzeneboronic Acid serves as a critical reagent in the selective functionalization of aromatic compounds. Its ability to undergo various transformations, such as halogenation, alkylation, and arylation, makes it an indispensable tool for modifying organic molecules with precision. This versatility extends its utility to diverse areas of chemical research and development, including medicinal chemistry and materials science.Overall, the strategic use of 3,4-Difluorobenzeneboronic Acid in chemical synthesis showcases its significance as a valuable reagent for achieving synthetic goals efficiently and effectively.