1217500-89-4 | 3-Chloro-2-isobutoxypyridine-5-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$60.00	$42.00
250mg	98%	in stock	$95.00	$66.00
1g	98%	in stock	$105.00	$74.00
5g	98%	in stock	$297.00	$208.00
10g	98%	in stock	$448.00	$314.00
25g	98%	in stock	$758.00	$531.00

Description

• Catalog Number: AA53942
• Chemical Name: 3-Chloro-2-isobutoxypyridine-5-boronic acid
• CAS Number: 1217500-89-4
• Molecular Formula: C9H13BClNO3
• Molecular Weight: 229.4684
• MDL Number: MFCD28040882
• SMILES: CC(COc1ncc(cc1Cl)B(O)O)C

Computed Properties

• Complexity: 194
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Upstream Synthesis Route

In chemical synthesis, (5-Chloro-6-isobutoxypyridin-3-yl)boronic acid serves as a versatile building block for the creation of various functionalized organic molecules. This compound is frequently utilized in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid source to form carbon-carbon bonds. The boronic acid functionality enables selective and efficient coupling with aryl halides or pseudohalides under mild reaction conditions. Additionally, (5-Chloro-6-isobutoxypyridin-3-yl)boronic acid can participate in transition-metal-catalyzed reactions to introduce the pyridinyl fragment into complex molecular structures. Its ability to undergo diverse transformations makes it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.