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CAS 850567-99-6

:

{3-[(E)-2-nitroethenyl]phenyl}boronic acid

Description:
{3-[(E)-2-nitroethenyl]phenyl}boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a nitro-substituted vinyl group attached to a phenyl ring. This compound typically exhibits properties such as moderate solubility in polar organic solvents and potential reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling and other cross-coupling reactions. The presence of the nitro group introduces electron-withdrawing characteristics, which can influence the compound's reactivity and stability. Additionally, the compound may exhibit unique optical properties due to its conjugated system, making it of interest in materials science and organic synthesis. Its applications may extend to medicinal chemistry, where boronic acids are often utilized for drug development and as intermediates in the synthesis of biologically active compounds. Overall, {3-[(E)-2-nitroethenyl]phenyl}boronic acid represents a versatile building block in organic synthesis and materials chemistry.
Formula:C8H8BNO4
InChI:InChI=1/C8H8BNO4/c11-9(12)8-3-1-2-7(6-8)4-5-10(13)14/h1-6,11-12H/b5-4+
Synonyms:
  • {3-[(E)-2-Nitrovinyl]phenyl}boronic acid
  • boronic acid, B-[3-[(E)-2-nitroethenyl]phenyl]-
  • (E)-(3-(2-Nitrovinyl)phenyl)boronicacid
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