1217501-12-6 | 2-Bromo-4-fluorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$14.00	$10.00
1g	98%	in stock	$23.00	$17.00
5g	98%	in stock	$112.00	$79.00
10g	98%	in stock	$191.00	$134.00
25g	98%	in stock	$477.00	$334.00
100g	98%	in stock	$1,878.00	$1,315.00

Description

• Catalog Number: AA53921
• Chemical Name: 2-Bromo-4-fluorophenylboronic acid
• CAS Number: 1217501-12-6
• Molecular Formula: C6H5BBrFO2
• Molecular Weight: 218.8161
• MDL Number: MFCD13195647
• SMILES: Fc1ccc(c(c1)Br)B(O)O

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

(2-Bromo-4-fluorophenyl)boronic acid, a versatile organic compound, plays a crucial role in chemical synthesis, particularly in the field of organic chemistry as a valuable building block. This compound is frequently employed in the construction of various pharmaceuticals, agricultural chemicals, and materials due to its unique chemical properties. One of the primary applications of (2-Bromo-4-fluorophenyl)boronic acid is its utility as a valuable reagent in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, facilitates the formation of carbon-carbon bonds between an aryl halide and an aryl or vinyl boronic acid, resulting in the synthesis of complex organic molecules. The high reactivity and selectivity of (2-Bromo-4-fluorophenyl)boronic acid make it an ideal substrate for these important coupling reactions, enabling the efficient assembly of various organic compounds with diverse functionalities.Moreover, (2-Bromo-4-fluorophenyl)boronic acid can also be utilized in the preparation of boron-containing building blocks, which serve as key intermediates in the synthesis of biologically active compounds and functional materials. Its strategic incorporation into molecular structures allows for the modulation of their physicochemical properties, contributing to the development of new drugs, agrochemicals, and advanced materials.In summary, (2-Bromo-4-fluorophenyl)boronic acid emerges as a valuable tool in the arsenal of synthetic chemists, enabling the construction of complex molecules through innovative chemical transformations. Its versatile applications in Suzuki-Miyaura cross-coupling reactions and the synthesis of functionalized organic compounds highlight its significance in advancing chemical synthesis and molecular design.