166330-03-6 | Bromomethylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$6.00	$5.00
5g	96%	in stock	$11.00	$8.00
10g	96%	in stock	$18.00	$13.00
25g	96%	in stock	$39.00	$28.00
100g	96%	in stock	$155.00	$109.00

Description

• Catalog Number: AA88780
• Chemical Name: Bromomethylboronic acid pinacol ester
• CAS Number: 166330-03-6
• Molecular Formula: C7H14BBrO2
• Molecular Weight: 220.89986
• MDL Number: MFCD09271779
• SMILES: BrCB1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 143
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

The compound 1,3,2-Dioxaborolane, 2-(bromomethyl)-4,4,5,5-tetramethyl- is a versatile reagent used in various chemical synthesis processes. It serves as a valuable building block in organic chemistry, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. This compound is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique reactivity and ability to facilitate challenging transformations. Its strategic placement of boron and bromine atoms enables it to participate in key reactions such as Suzuki-Miyaura cross-coupling, palladium-catalyzed reactions, and other transformations that are crucial for the construction of complex molecular structures. Additionally, the tetramethyl groups provide steric protection and influence the compound's overall reactivity, making it a valuable tool in modern organic synthesis strategies.