1072951-95-1 | 2-Bromo-3-butoxy-6-fluorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$10.00	$7.00
250mg	98%	in stock	$23.00	$16.00
1g	98%	in stock	$66.00	$46.00
5g	98%	in stock	$260.00	$182.00

Description

• Catalog Number: AB61317
• Chemical Name: 2-Bromo-3-butoxy-6-fluorophenylboronic acid
• CAS Number: 1072951-95-1
• Molecular Formula: C10H13BBrFO3
• Molecular Weight: 290.9218
• MDL Number: MFCD08276824
• SMILES: CCCCOc1ccc(c(c1Br)B(O)O)F

Computed Properties

• Complexity: 209
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5

Upstream Synthesis Route

The compound (2-Bromo-3-butoxy-6-fluorophenyl)boronic acid is a versatile building block widely used in chemical synthesis. Its unique structure and reactivity make it an essential reagent in various organic transformations, particularly in the field of medicinal chemistry and materials science.One of the key applications of (2-Bromo-3-butoxy-6-fluorophenyl)boronic acid in chemical synthesis is in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by a palladium catalyst, allows for the formation of carbon-carbon bonds between an aryl or heteroaryl boronic acid and an aryl or vinyl halide. The boronic acid functionality in (2-Bromo-3-butoxy-6-fluorophenyl)boronic acid serves as a crucial partner in this coupling process, enabling the construction of complex organic molecules with high efficiency and selectivity.Additionally, (2-Bromo-3-butoxy-6-fluorophenyl)boronic acid can also be employed in the synthesis of biologically active compounds and pharmaceutical intermediates. Its ability to participate in diverse carbon-carbon and carbon-heteroatom bond-forming reactions makes it a valuable tool for organic chemists seeking to access novel molecular scaffolds for drug discovery and development.Overall, the importance of (2-Bromo-3-butoxy-6-fluorophenyl)boronic acid in chemical synthesis lies in its versatility and compatibility with various reaction conditions, enabling the rapid and efficient construction of complex organic molecules with potential applications in a wide range of scientific disciplines.