1218790-62-5 | 3,5-Dichloro-4-isopropoxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$165.00	$115.00
1g	97%	in stock	$198.00	$138.00
5g	97%	in stock	$572.00	$400.00
25g	97%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AA54574
• Chemical Name: 3,5-Dichloro-4-isopropoxyphenylboronic acid
• CAS Number: 1218790-62-5
• Molecular Formula: C9H11BCl2O3
• Molecular Weight: 248.8988
• MDL Number: MFCD15143466
• SMILES: OB(c1cc(Cl)c(c(c1)Cl)OC(C)C)O

Computed Properties

• Complexity: 192
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

$Name$ is a versatile compound that finds wide application in chemical synthesis, particularly in the field of organic chemistry. One key role of (3,5-Dichloro-4-isopropoxyphenyl)boronic acid is as a building block for the preparation of various pharmaceuticals, agrochemicals, and materials. Its boronic acid functional group allows for efficient and selective cross-coupling reactions with suitable electrophiles, leading to the formation of complex molecular structures. This compound is instrumental in the construction of carbon-carbon and carbon-heteroatom bonds, enabling chemists to access a diverse array of organic molecules with specific properties and functions. Furthermore, (3,5-Dichloro-4-isopropoxyphenyl)boronic acid plays a crucial role in medicinal chemistry by facilitating the synthesis of potential drug candidates with enhanced biological activities. Its incorporation in synthetic routes allows for the strategic introduction of functional groups and stereochemistry, contributing to the development of novel therapeutic agents. In addition to its synthetic utility, this compound serves as a valuable tool in mechanistic studies, exploring new reaction pathways and driving innovation in the field of chemical synthesis.