1055881-23-6 | 2-Formylfuran-3-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$89.00	$62.00
1g	98%	in stock	$201.00	$141.00
5g	98%	in stock	$758.00	$531.00
10g	98%	in stock	$1,317.00	$922.00
25g	98%	in stock	$2,623.00	$1,836.00

Description

• Catalog Number: AE12852
• Chemical Name: 2-Formylfuran-3-boronic acid pinacol ester
• CAS Number: 1055881-23-6
• Molecular Formula: C11H15BO4
• Molecular Weight: 222.0454
• MDL Number: MFCD07368242
• SMILES: O=Cc1occc1B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 274
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2

Upstream Synthesis Route

The 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehyde is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the synthesis of various organic molecules and materials due to its functional groups and structural features.One significant application of 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehyde is in the formation of C-C and C-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions. Its boron functionality allows for efficient and selective coupling with a range of aryl and heteroaryl halides or pseudohalides, enabling the rapid construction of complex molecular structures.Furthermore, this compound can also participate in various transformations such as hydroformylation, allylation, and other carbon-carbon bond-forming reactions, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its ability to introduce diverse functional groups and control stereochemistry makes it a crucial component in modern organic synthesis strategies.