1072952-42-1 | 5-Chloro-2-fluoro-4-methylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$15.00	$10.00
250mg	95%	in stock	$20.00	$14.00
1g	95%	in stock	$45.00	$31.00
5g	95%	in stock	$163.00	$114.00
25g	95%	in stock	$605.00	$423.00
100g	95%	in stock	$2,004.00	$1,403.00

Description

• Catalog Number: AD79395
• Chemical Name: 5-Chloro-2-fluoro-4-methylphenylboronic acid
• CAS Number: 1072952-42-1
• Molecular Formula: C7H7BClFO2
• Molecular Weight: 188.3917
• MDL Number: MFCD07368241
• SMILES: OB(c1cc(Cl)c(cc1F)C)O

Computed Properties

• Complexity: 158
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

B-(5-Chloro-2-fluoro-4-methylphenyl)boronic acid is a versatile chemical compound widely utilized in chemical synthesis as a key building block. This boronic acid derivative is particularly valuable in the field of organic chemistry due to its ability to participate in various cross-coupling reactions, including Suzuki-Miyaura coupling, which is a powerful method for the formation of carbon-carbon bonds.In the realm of drug discovery and development, B-(5-Chloro-2-fluoro-4-methylphenyl)boronic acid plays a crucial role in the synthesis of pharmaceutical intermediates and active ingredients. Its unique structure and reactivity make it a valuable tool for the construction of complex molecular architectures. Additionally, this compound finds applications in the synthesis of advanced materials, such as polymers and liquid crystals, where precise control over the chemical structure is essential for achieving desired properties.Furthermore, B-(5-Chloro-2-fluoro-4-methylphenyl)boronic acid is employed in the preparation of functionalized organic molecules for use in agrochemicals, materials science, and other industrial applications. Its compatibility with various reaction conditions and wide substrate scope make it a versatile reagent for chemists seeking to streamline and diversify their synthetic routes.