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CAS 102170-51-4

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B-[3-(Aminocarbonyl)-5-nitrophenyl]boronic acid

Description:
B-[3-(Aminocarbonyl)-5-nitrophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features both an aminocarbonyl and a nitro substituent. This compound typically exhibits properties such as moderate solubility in polar solvents due to the presence of the boronic acid group, which can engage in hydrogen bonding. The aminocarbonyl group contributes to its potential reactivity, allowing for interactions with various electrophiles, while the nitro group can influence the electronic properties of the molecule, potentially enhancing its reactivity in certain chemical reactions. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis and medicinal chemistry. Additionally, this compound may have applications in the development of pharmaceuticals, particularly in the context of targeted drug delivery or as intermediates in the synthesis of more complex molecules. Overall, its unique structural features make it a compound of interest in both research and industrial applications.
Formula:C7H7BN2O5
InChI:InChI=1S/C7H7BN2O5/c9-7(11)4-1-5(8(12)13)3-6(2-4)10(14)15/h1-3,12-13H,(H2,9,11)
InChI key:InChIKey=XELWZRCEJDUTEC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=O)=CC(N(=O)=O)=C1
Synonyms:
  • (3-Carbamoyl-5-nitrophenyl)boronic acid
  • 3-(Aminocarbonyl)-5-Nitrobenzeneboronic Acid
  • 3-(Aminocarbonyl)-5-nitrobenzeneboronic acid 98%
  • 3-Aminocarbonyl-5-Nitrophenylboronic Acid
  • 3-Borono-5-Nitrobenzamide
  • 3-Carbamoyl-5-nitrobenzeneboronic acid
  • B-[3-(Aminocarbonyl)-5-nitrophenyl]boronic acid
  • Benzeneboronic Acid, 3-Carbamoyl-5-Nitro-
  • Boronic acid, B-[3-(aminocarbonyl)-5-nitrophenyl]-
  • Boronic acid, [3-(aminocarbonyl)-5-nitrophenyl]-
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