1083168-96-0 | 5-Chloro-2-methoxypyridine-3-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$45.00	$31.00
250mg	96%	in stock	$75.00	$52.00
1g	96%	in stock	$208.00	$145.00
5g	96%	in stock	$738.00	$516.00
10g	96%	in stock	$1,341.00	$939.00
25g	96%	in stock	$2,580.00	$1,806.00

Description

• Catalog Number: AD43337
• Chemical Name: 5-Chloro-2-methoxypyridine-3-boronic acid pinacol ester
• CAS Number: 1083168-96-0
• Molecular Formula: C12H17BClNO3
• Molecular Weight: 269.5323
• MDL Number: MFCD09878898
• SMILES: COc1ncc(cc1B1OC(C(O1)(C)C)(C)C)Cl

Computed Properties

• Complexity: 298
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2

Upstream Synthesis Route

5-Chloro-2-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound widely utilized in chemical synthesis as a key building block. This compound plays a crucial role in various organic reactions such as Suzuki coupling, a popular cross-coupling reaction used in the formation of carbon-carbon bonds. By incorporating this compound into the reaction mixture, chemists can efficiently create complex organic molecules by coupling different functional groups together. Its strategic placement within the pyridine ring enables precise control over the regioselectivity and functional group compatibility in the synthetic pathway, leading to the formation of diverse molecular structures with high efficiency and purity. Furthermore, the unique boron-containing moiety enhances the stability and reactivity of the compound, making it an indispensable tool in modern organic synthesis strategies.