1056475-66-1 | 3-Methylsulfinylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$100.00	$70.00
250mg	95%	in stock	$155.00	$109.00
1g	95%	in stock	$265.00	$186.00
5g	95%	in stock	$758.00	$531.00
10g	95%	in stock	$1,317.00	$922.00
25g	95%	in stock	$2,623.00	$1,836.00

Description

• Catalog Number: AD44513
• Chemical Name: 3-Methylsulfinylphenylboronic acid
• CAS Number: 1056475-66-1
• Molecular Formula: C7H9BO3S
• Molecular Weight: 184.0206
• MDL Number: MFCD03092931
• SMILES: OB(c1cccc(c1)S(=O)C)O

Computed Properties

• Complexity: 174
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• Undefined Atom Stereocenter Count: 1

Upstream Synthesis Route

With its unique chemical structure, (3-(Methylsulfinyl)phenyl)boronic acid serves as a versatile building block in organic synthesis. This compound is commonly utilized in the formation of carbon-carbon and carbon-heteroatom bonds, making it a valuable reagent in various chemical reactions.One key application of (3-(Methylsulfinyl)phenyl)boronic acid is its role in Suzuki-Miyaura cross-coupling reactions. This important synthetic method involves the coupling of an aryl halide or pseudohalide with an organoboron compound, such as (3-(Methylsulfinyl)phenyl)boronic acid, to create biaryl structures. The ability of (3-(Methylsulfinyl)phenyl)boronic acid to participate in such transformations highlights its significance in the assembly of complex organic molecules.Furthermore, (3-(Methylsulfinyl)phenyl)boronic acid can also be employed in metal-catalyzed reactions, including palladium-catalyzed C-H functionalization. By serving as a boronate ester source, this compound enables the selective introduction of aryl groups onto various substrates, thereby expanding the synthetic toolbox for chemists.In addition to its use in traditional cross-coupling reactions, (3-(Methylsulfinyl)phenyl)boronic acid has been applied in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties. Its versatility and compatibility with a range of reaction conditions make it a valuable reagent for chemists seeking to construct intricate molecular architectures with precision and efficiency.