1160790-84-0 | 1-Methyl-2-oxo-1,2-dihydropyridin-4-ylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$70.00	$49.00
500mg	98%	in stock	$118.00	$83.00
1g	98%	in stock	$190.00	$133.00
5g	98%	in stock	$674.00	$472.00

Description

• Catalog Number: AA14801
• Chemical Name: 1-Methyl-2-oxo-1,2-dihydropyridin-4-ylboronic acid pinacol ester
• CAS Number: 1160790-84-0
• Molecular Formula: C12H18BNO3
• Molecular Weight: 235.0872
• MDL Number: MFCD12032569
• SMILES: Cn1ccc(cc1=O)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 396
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. With its unique structure containing a boron heterocycle, $name$ serves as a valuable building block in the preparation of various organic molecules.In chemical synthesis, $name$ plays a crucial role as a boronic ester derivative, offering a convenient platform for Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, enables the formation of carbon-carbon bonds, making it a powerful tool in creating complex and functionalized organic compounds. By incorporating $name$ into the reaction sequence, chemists can efficiently introduce the pyridine moiety while harnessing the reactivity of the boron functionality for further functionalization.Furthermore, the presence of the pyridine ring in $name$ confers unique properties to the synthesized molecules, allowing for potential applications in the development of pharmaceuticals, agrochemicals, and materials science. By leveraging the versatility of $name$ in chemical synthesis, researchers can access a diverse array of compounds with tailored properties and activities, making it a key component in the toolkit of synthetic chemists.