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CAS 1256345-63-7

:

B-(4-Acetyl-3-nitrophenyl)boronic acid

Description:
B-(4-Acetyl-3-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 acetyl and a nitro substituent. This compound typically exhibits properties such as moderate solubility in polar organic solvents and can participate in various chemical reactions, including Suzuki-Miyaura cross-coupling reactions, which are significant in organic synthesis for forming carbon-carbon bonds. The presence of the acetyl group contributes to its reactivity, while the nitro group can influence electronic properties and sterics. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in sensing applications and in the development of drug delivery systems. The compound's structure suggests potential applications in medicinal chemistry and materials science, particularly in the synthesis of complex organic molecules. As with many boronic acids, care should be taken in handling due to potential reactivity and the need for proper storage conditions to maintain stability.
Formula:C8H8BNO5
InChI:InChI=1S/C8H8BNO5/c1-5(11)7-3-2-6(9(12)13)4-8(7)10(14)15/h2-4,12-13H,1H3
InChI key:InChIKey=PZXBGJTWRHMQQR-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(C(C)=O)C=CC(B(O)O)=C1
Synonyms:
  • B-(4-Acetyl-3-nitrophenyl)boronic acid
  • Boronic acid, B-(4-acetyl-3-nitrophenyl)-
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