1010101-08-2 | 2,6-Dichloro-3-methylpyridine-4-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$299.00	$209.00
1g	95%	in stock	$713.00	$499.00

Description

• Catalog Number: AI05134
• Chemical Name: 2,6-Dichloro-3-methylpyridine-4-boronic acid pinacol ester
• CAS Number: 1010101-08-2
• Molecular Formula: C12H16BCl2NO2
• Molecular Weight: 287.9779
• MDL Number: MFCD11617878
• SMILES: Clc1nc(Cl)c(c(c1)B1OC(C(O1)(C)C)(C)C)C

Computed Properties

• Complexity: 311
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

2,6-Dichloro-3-methylpyridine-4-boronic acid pinacol ester is a versatile chemical compound widely used in organic synthesis. This advanced reagent serves as a key building block in the preparation of various functionalized organic compounds. Its unique structure provides an ideal platform for the selective introduction of boronic acid moieties into complex molecular structures.In chemical synthesis, 2,6-Dichloro-3-methylpyridine-4-boronic acid pinacol ester plays a crucial role in Suzuki-Miyaura cross-coupling reactions. By serving as a boronate ester source, this compound facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl and heteroaryl compounds. Furthermore, its pyridine core offers additional reactivity and versatility, allowing for the functionalization of aromatic systems with high selectivity.Additionally, the pinacol ester group in this compound provides stability and solubility, making it well-suited for use in various organic transformations. From pharmaceuticals to agrochemicals, the application of 2,6-Dichloro-3-methylpyridine-4-boronic acid pinacol ester in chemical synthesis enables the efficient construction of diverse molecular scaffolds with tailored properties and functionalities.