[3-(Diethylsulfamoyl)-4-methoxy-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features a methoxy group and a diethylsulfamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxy group can enhance solubility and influence the electronic properties of the molecule, while the diethylsulfamoyl group may impart specific biological activity or enhance interactions with biological targets. The compound is likely to be a solid at room temperature, with potential applications in drug development, particularly in the design of inhibitors for certain enzymes or receptors. Its reactivity and stability can be influenced by pH and the presence of other functional groups in a reaction environment. As with many boronic acids, it may also participate in cross-coupling reactions, making it valuable in synthetic organic chemistry.

[3-(diethylsulfamoyl)-4-methoxy-phenyl]boronic acid

871333-03-8: [3-(Diethylsulfamoyl)-4-methoxy-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features a methoxy group and a diethylsulfamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the methoxy group can enhance solubility and influence the electronic properties of the molecule, while the diethylsulfamoyl group may impart specific biological activity or enhance interactions with biological targets. The compound is likely to be a solid at room temperature, with potential applications in drug development, particularly in the design of inhibitors for certain enzymes or receptors. Its reactivity and stability can be influenced by pH and the presence of other functional groups in a reaction environment. As with many boronic acids, it may also participate in cross-coupling reactions, making it valuable in synthetic organic chemistry.

CAS 871333-03-8

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