1073353-98-6 | 2,5-Dichloropyridine-4-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$53.00	$37.00
1g	95%	in stock	$121.00	$85.00
5g	95%	in stock	$429.00	$300.00
10g	95%	in stock	$851.00	$596.00
25g	95%	in stock	$1,403.00	$982.00

Description

• Catalog Number: AD68502
• Chemical Name: 2,5-Dichloropyridine-4-boronic acid, pinacol ester
• CAS Number: 1073353-98-6
• Molecular Formula: C11H14BCl2NO2
• Molecular Weight: 273.9514
• MDL Number: MFCD06798256
• SMILES: CC1(C)OB(OC1(C)C)c1cc(Cl)ncc1Cl

Computed Properties

• Complexity: 285
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

2,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound commonly used in chemical synthesis. This compound serves as an important building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.In chemical synthesis, 2,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine acts as a key reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is widely utilized in the formation of carbon-carbon bonds, allowing chemists to efficiently construct complex organic molecules. By serving as a coupling partner in this reaction, 2,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine facilitates the synthesis of diverse chemical structures with high efficiency and selectivity.Furthermore, this compound's compatibility with various functional groups and its stability under a wide range of reaction conditions make it a valuable tool in organic synthesis. Chemists leverage its reactivity and reliability to streamline the synthesis of target molecules, making it an indispensable component in the toolkit of synthetic chemists worldwide.