1083168-93-7 | 2-Methoxy-3-(carbomethoxy)pyridine-5-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$23.00	$16.00
250mg	96%	in stock	$27.00	$19.00
1g	96%	in stock	$98.00	$69.00
25g	96%	in stock	$1,955.00	$1,368.00
100g	96%	in stock	$6,198.00	$4,339.00

Description

• Catalog Number: AB75635
• Chemical Name: 2-Methoxy-3-(carbomethoxy)pyridine-5-boronic acid, pinacol ester
• CAS Number: 1083168-93-7
• Molecular Formula: C14H20BNO5
• Molecular Weight: 293.1233
• MDL Number: MFCD11855973
• SMILES: COC(=O)c1cc(cnc1OC)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 385
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4

Upstream Synthesis Route

Methyl 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate is a valuable compound utilized in chemical synthesis for the efficient incorporation of the nicotinic moiety into various organic molecules. Its strategic placement of the boronate ester group allows for selective and controlled cross-coupling reactions, particularly in palladium-catalyzed processes.This compound serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to participate in Suzuki-Miyaura cross-coupling reactions. Through these transformations, complex molecular structures can be constructed with high efficiency and selectivity, making it a valuable tool for medicinal chemists and process chemists alike.Additionally, the presence of the methoxy and methyl substituents on the nicotinic core provides flexibility for further derivatization, allowing for the fine-tuning of physical and chemical properties in target molecules. Overall, Methyl 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate plays a crucial role in modern organic synthesis, enabling the streamlined construction of diverse functionalized compounds for various applications.