[3-(Diethylcarbamoyl)-5-nitro-phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a nitrophenyl moiety, which can enhance its reactivity and solubility in organic solvents. The diethylcarbamoyl group contributes to the compound's overall stability and may influence its biological activity. Typically, boronic acids exhibit moderate to high solubility in polar organic solvents, and their reactivity can be modulated by the substituents on the aromatic ring. This compound may also exhibit interesting properties such as fluorescence or catalytic activity, depending on its specific structure and environment. Its applications may extend to drug development, particularly in the design of inhibitors for various biological targets, owing to the versatility of boronic acids in forming complexes with biomolecules.

[3-(diethylcarbamoyl)-5-nitro-phenyl]boronic acid

871332-82-0: [3-(Diethylcarbamoyl)-5-nitro-phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a nitrophenyl moiety, which can enhance its reactivity and solubility in organic solvents. The diethylcarbamoyl group contributes to the compound's overall stability and may influence its biological activity. Typically, boronic acids exhibit moderate to high solubility in polar organic solvents, and their reactivity can be modulated by the substituents on the aromatic ring. This compound may also exhibit interesting properties such as fluorescence or catalytic activity, depending on its specific structure and environment. Its applications may extend to drug development, particularly in the design of inhibitors for various biological targets, owing to the versatility of boronic acids in forming complexes with biomolecules.

(3-(Diethylcarbamoyl)-5-nitrophenyl)boronic acid

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CAS 871332-82-0

[3-(diethylcarbamoyl)-5-nitro-phenyl]boronic acid

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Ref: IN-DA004TVF

3-(Diethylcarbamoyl)-5-nitrobenzeneboronic acid

Ref: 54-OR9434

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Ref: 10-F215010