1217501-41-1 | 5-Chloro-2-isopropoxypyridine-3-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$53.00	$37.00
250mg	96%	in stock	$85.00	$59.00
1g	96%	in stock	$203.00	$142.00
5g	96%	in stock	$573.00	$402.00
10g	96%	in stock	$946.00	$662.00
25g	96%	in stock	$1,879.00	$1,316.00

Description

• Catalog Number: AA53989
• Chemical Name: 5-Chloro-2-isopropoxypyridine-3-boronic acid
• CAS Number: 1217501-41-1
• Molecular Formula: C8H11BClNO3
• Molecular Weight: 215.4418
• MDL Number: MFCD13195662
• SMILES: CC(Oc1ncc(cc1B(O)O)Cl)C

Computed Properties

• Complexity: 182
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

Utilizing its unique structural properties, (5-Chloro-2-isopropoxypyridin-3-yl)boronic acid serves as a valuable building block in chemical synthesis. This compound plays a crucial role in modern organic chemistry as a versatile reagent, particularly in the formation of carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions. Additionally, it is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and materials science due to its ability to introduce the pyridine motif with a chloro substituent at the 5th position. The presence of the boronic acid group facilitates the formation of stable boronate esters, enabling further functionalization and derivatization of the molecule. As a result, the incorporation of (5-Chloro-2-isopropoxypyridin-3-yl)boronic acid into synthetic pathways offers a powerful tool for the construction of complex molecular frameworks with diverse applications in the field of organic chemistry.