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CAS 850568-46-6

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B-(4-Cyano-2-nitrophenyl)boronic acid

Description:
B-(4-Cyano-2-nitrophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that bears both a cyano and a nitro substituent. This compound typically exhibits a crystalline solid form and is soluble in polar organic solvents. The presence of the boronic acid group allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The cyano group contributes to the compound's electronic properties, potentially enhancing its reactivity, while the nitro group can influence its polarity and solubility. Additionally, this compound may exhibit interesting biological activities, making it a subject of interest in pharmaceutical research. Its stability under standard laboratory conditions is generally good, but care should be taken to avoid moisture, as boronic acids can hydrolyze. Overall, B-(4-Cyano-2-nitrophenyl)boronic acid serves as a versatile building block in the synthesis of more complex organic molecules.
Formula:C7H5BN2O4
InChI:InChI=1S/C7H5BN2O4/c9-4-5-1-2-6(8(11)12)7(3-5)10(13)14/h1-3,11-12H
InChI key:InChIKey=YDIOTBNYNPBRFF-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(B(O)O)C=CC(C#N)=C1
Synonyms:
  • B-(4-Cyano-2-nitrophenyl)boronic acid
  • Boronic acid, (4-cyano-2-nitrophenyl)-
  • boronic acid, B-(4-cyano-2-nitrophenyl)-
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