1042443-60-6 | 2-Ethylsulfonylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$251.00	$176.00
1g	97%	in stock	$558.00	$391.00

Description

• Catalog Number: AD50003
• Chemical Name: 2-Ethylsulfonylphenylboronic acid
• CAS Number: 1042443-60-6
• Molecular Formula: C8H11BO4S
• Molecular Weight: 214.0465
• MDL Number: MFCD03095198
• SMILES: CCS(=O)(=O)c1ccccc1B(O)O

Computed Properties

• Complexity: 270
• 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

(2-(Ethylsulfonyl)phenyl)boronic acid is a versatile organic compound commonly employed in chemical synthesis as a valuable building block. Its unique properties and reactivity make it a popular choice in various applications within the field of organic chemistry. One of the primary uses of (2-(Ethylsulfonyl)phenyl)boronic acid is as a key component in Suzuki-Miyaura cross-coupling reactions. This reaction, named after its discovery by Akira Suzuki and Noboru Miyaura, is a fundamental method for forming carbon-carbon bonds in organic synthesis. By utilizing (2-(Ethylsulfonyl)phenyl)boronic acid as a boronate ester partner, alongside an aryl halide or pseudohalide partner, chemists can efficiently construct biaryl compounds with high regioselectivity and excellent yields. This reaction has wide-ranging applications in pharmaceuticals, agrochemicals, materials science, and other industries.Furthermore, the boronic acid functionality in (2-(Ethylsulfonyl)phenyl)boronic acid also enables it to participate in various other transformations, such as C-H activation reactions, hydroboration, and metal-catalyzed coupling reactions. These diverse chemical reactions showcase the versatility of (2-(Ethylsulfonyl)phenyl)boronic acid as a powerful tool for organic chemists seeking to synthesize complex molecular structures with precision and efficiency.