68162-47-0 | 4-Bromomethylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$5.00	$4.00
5g	98%	in stock	$17.00	$12.00
10g	98%	in stock	$30.00	$21.00
25g	98%	in stock	$70.00	$49.00
100g	98%	in stock	$240.00	$168.00

Description

• Catalog Number: AB48336
• Chemical Name: 4-Bromomethylphenylboronic acid
• CAS Number: 68162-47-0
• Molecular Formula: C7H8BBrO2
• Molecular Weight: 214.8522
• MDL Number: MFCD01318113
• SMILES: BrCc1ccc(cc1)B(O)O

Computed Properties

• Complexity: 113
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

4-(Bromomethyl)phenylboronic acid is a versatile chemical compound widely utilized in organic synthesis for its unique properties and reactivity. In chemical synthesis, this compound serves as a crucial building block for the introduction of the phenylboronic acid moiety into various organic molecules. Its bromomethyl group enables selective functionalization and modification of organic compounds through cross-coupling reactions, such as Suzuki-Miyaura coupling, facilitating the formation of complex molecular structures. Furthermore, the boronic acid functionality in 4-(Bromomethyl)phenylboronic acid allows for the creation of arylboronic esters, enabling further diversification of chemical compounds for various applications in medicinal chemistry, material science, and agrochemicals. Widely recognized for its role as a key reagent in modern organic synthesis, 4-(Bromomethyl)phenylboronic acid continues to play a vital role in advancing the field of chemical research and development.

Literature

• Structure-based design of novel boronic acid-based inhibitors of autotaxin.

  Journal of medicinal chemistry 20110714

• Enhanced gene transfection capability of polyethylenimine by incorporating boronic acid groups.

  Chemical communications (Cambridge, England) 20100828