[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.

[4-(benzylsulfamoyl)phenyl]boronic acid

548769-96-6: [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.

CAS 548769-96-6

[4-(benzylsulfamoyl)phenyl]boronic acid

N-Benzyl 4-boronobenzenesulfonamide

Ref: IN-DA00DABY

4-(N-Benzylsulphonamido)benzeneboronic acid

Ref: 54-OR4116

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

Ref: 10-F235431