CAS 193753-37-6: Boronic acid, [2-(aminosulfonyl)phenyl]-

Description: Boronic acid, [2-(aminosulfonyl)phenyl]-, with the CAS number 193753-37-6, is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains an aminosulfonyl substituent. This compound typically exhibits properties associated with both boronic acids and sulfonamides, including the ability to form reversible covalent bonds with diols, which makes it useful in various applications such as drug development and materials science. The aminosulfonyl group contributes to its solubility in polar solvents and may enhance its biological activity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, making this compound potentially valuable in synthetic organic chemistry. Its structural features suggest that it may participate in hydrogen bonding and other intermolecular interactions, influencing its reactivity and stability. Overall, [2-(aminosulfonyl)phenyl]boronic acid is a versatile compound with applications in medicinal chemistry and materials science.

Formula: C₆H₈BNO₄S

2-Boronobenzenesulfonamide

CAS: 193753-37-6

• Formula: C₆H₈BNO₄S
• Molecular weight: 201.0080

2-Boronobenzenesulfonamide

CAS: 193753-37-6

• Molecular weight: 201.01g/mol

(2-Sulfamoylphenyl)boronic acid

CAS: 193753-37-6

• Purity: 98%
• Molecular weight: 201.0

2-Boronobenzenesulfonamide

CAS: 193753-37-6

Versatile small molecule scaffold

• Formula: C₆H₈BNO₄S
• Purity: Min. 95%
• Molecular weight: 201.01 g/mol