1054483-78-1 | 6-Hydroxypyridine-3-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$9.00	$7.00
250mg	97%	in stock	$12.00	$9.00
1g	97%	in stock	$25.00	$18.00
5g	97%	in stock	$120.00	$84.00
10g	97%	in stock	$239.00	$168.00
25g	97%	in stock	$532.00	$373.00

Description

• Catalog Number: AB50584
• Chemical Name: 6-Hydroxypyridine-3-boronic acid, pinacol ester
• CAS Number: 1054483-78-1
• Molecular Formula: C11H16BNO3
• Molecular Weight: 221.0606
• MDL Number: MFCD06795671
• SMILES: O=c1ccc(c[nH]1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 369
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1

Upstream Synthesis Route

The chemical compound $name$, also known as 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ol, is widely used in chemical synthesis for its versatile applications. As a key reagent in organic chemistry, $name$ serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and functional groups make it a crucial component in the preparation of complex organic molecules through cross-coupling reactions, such as Suzuki-Miyaura coupling and Negishi coupling.$name$ plays a pivotal role in the formation of carbon-carbon and carbon-heteroatom bonds, enabling chemists to efficiently construct intricate molecular architectures. By serving as a boronic acid derivative, $name$ facilitates the introduction of pyridine and alcohol moieties into target molecules, offering synthetic chemists a powerful tool for achieving precise structural modifications. Its compatibility with a wide range of functional groups and reaction conditions further enhances its utility in diverse synthetic transformations, making it a valuable asset in the arsenal of modern organic chemists.