CAS 548769-96-6: [4-(benzylsulfamoyl)phenyl]boronic acid

Description: [4-(Benzylsulfamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group and a sulfamoyl moiety. It features a phenyl ring substituted with a benzylsulfamoyl group, which enhances its solubility and reactivity. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. This compound may exhibit properties such as moderate to high solubility in polar solvents and potential biological activity due to the presence of the sulfamoyl group, which can interact with biological targets. Additionally, its structure suggests potential applications in medicinal chemistry, particularly in the design of inhibitors or modulators of specific biological pathways. The compound's stability, reactivity, and interactions with other molecules can be influenced by factors such as pH and the presence of other functional groups. Overall, [4-(benzylsulfamoyl)phenyl]boronic acid represents a versatile building block in organic synthesis and pharmaceutical research.

Formula: C₁₃H₁₄BNO₄S

InChI: InChI=1/C13H14BNO4S/c16-14(17)12-6-8-13(9-7-12)20(18,19)15-10-11-4-2-1-3-5-11/h1-9,15-17H,10H2

4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID

CAS: 548769-96-6

• Formula: C₁₃H₁₄BNO₄S
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 291.1306

4-(N-Benzylsulphonamido)benzeneboronic acid

CAS: 548769-96-6

• Purity: 95%
• Color and Shape: White Solid
• Molecular weight: 291.13g/mol

(4-(N-Benzylsulfamoyl)phenyl)boronic acid

CAS: 548769-96-6

• Purity: 95.0%
• Molecular weight: 291.1300048828125

(4-(N-Benzylsulfamoyl)phenyl)boronic acid

CAS: 548769-96-6

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• Formula: C₁₃H₁₄BNO₄S
• Purity: Min. 95%
• Molecular weight: 291.13 g/mol