[3-(Benzyloxycarbonylamino)-5-nitro-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a nitro group and a benzyloxycarbonylamino group. 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 nitro group contributes to its electron-withdrawing characteristics, potentially influencing its reactivity and solubility in different solvents. The benzyloxycarbonylamino moiety enhances its stability and can facilitate interactions with biological targets. Overall, this compound is of interest in the development of pharmaceuticals and as a building block in organic synthesis due to its unique structural features and functional groups. Its specific reactivity and applications would depend on the context of its use in chemical reactions or biological systems.

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

874219-56-4: (3-{[(Benzyloxy)carbonyl]amino}-5-nitrophenyl)boronic acid

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CAS 874219-56-4: [3-(benzyloxycarbonylamino)-5-nitro-phenyl]boronic acid

3-Amino-5-nitrobenzeneboronic acid, CBZ protected

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3-Amino-5-nitrobenzeneboronic acid, CBZ protected

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(3-(((Benzyloxy)carbonyl)amino)-5-nitrophenyl)boronic acid

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(3-(((Benzyloxy)carbonyl)amino)-5-nitrophenyl)boronic acid

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