1003043-40-0 | 2-Chloro-3-methylpyridine-5-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$7.00	$5.00
1g	97%	in stock	$16.00	$11.00
5g	97%	in stock	$36.00	$26.00
25g	97%	in stock	$126.00	$88.00

Description

• Catalog Number: AA01798
• Chemical Name: 2-Chloro-3-methylpyridine-5-boronic acid
• CAS Number: 1003043-40-0
• Molecular Formula: C6H7BClNO2
• Molecular Weight: 171.3893
• MDL Number: MFCD03411564
• SMILES: OB(c1cnc(c(c1)C)Cl)O

Computed Properties

• Complexity: 136
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

(6-Chloro-5-methylpyridin-3-yl)boronic acid is a versatile chemical reagent widely used in organic synthesis. It serves as a valuable building block for the preparation of various functionalized molecules, particularly in the field of pharmaceuticals, agrochemicals, and materials science. In chemical synthesis, this boronic acid derivative can undergo Suzuki-Miyaura cross-coupling reactions with aryl or vinyl halides, leading to the formation of biaryl or polyaryl compounds. These reactions are fundamental in the construction of complex organic structures and are crucial in the development of pharmaceuticals and fine chemicals. Furthermore, (6-Chloro-5-methylpyridin-3-yl)boronic acid can also participate in other important transformations such as palladium-catalyzed C-H activation, borylation, and azidation reactions, providing access to a diverse range of substituted pyridine derivatives. Overall, the application of (6-Chloro-5-methylpyridin-3-yl)boronic acid in chemical synthesis enables chemists to efficiently access novel compounds with potential biological activities or functional properties, making it a valuable tool in modern organic chemistry research.