1004294-79-4 | 3-Hydroxy-5-(methoxycarbonyl)phenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$75.00	$52.00
250mg	97%	in stock	$118.00	$83.00
1g	97%	in stock	$313.00	$219.00
5g	97%	in stock	$964.00	$675.00

Description

• Catalog Number: AA02341
• Chemical Name: 3-Hydroxy-5-(methoxycarbonyl)phenylboronic acid, pinacol ester
• CAS Number: 1004294-79-4
• Molecular Formula: C14H19BO5
• Molecular Weight: 278.1087
• MDL Number: MFCD12546597
• SMILES: COC(=O)c1cc(cc(c1)O)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 366
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3

Upstream Synthesis Route

The compound Methyl 3-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate plays a crucial role in chemical synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in organic chemistry for the creation of carbon-carbon bonds, commonly used in the assembly of complex organic molecules. By serving as a boronic ester, Methyl 3-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate enables the selective formation of aryl-aryl or aryl-vinyl bonds under mild reaction conditions. This versatile compound facilitates the construction of diverse chemical structures with high efficiency and selectivity, making it a valuable component in the toolkit of synthetic chemists.