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CAS 216394-04-6

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trans-4-(beta-Nitrovinyl)benzeneboronic acid

Description:
Trans-4-(beta-Nitrovinyl)benzeneboronic acid is an organic compound characterized by the presence of a boronic acid functional group and a nitrovinyl substituent on a benzene ring. The compound features a trans configuration, indicating that the nitrovinyl group is positioned opposite to the boronic acid group across the benzene ring. This structural arrangement can influence its reactivity and interactions in chemical reactions, particularly in cross-coupling reactions and as a ligand in organometallic chemistry. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The nitrovinyl group can also participate in electrophilic reactions, enhancing the compound's versatility. Overall, trans-4-(beta-Nitrovinyl)benzeneboronic acid is a valuable compound in synthetic organic chemistry, with potential applications in medicinal chemistry and the development of new materials.
Formula:C8H8BNO4
InChI:InChI=1/C8H8BNO4/c11-9(12)8-3-1-7(2-4-8)5-6-10(13)14/h1-6,11-12H/b6-5+
Synonyms:
  • 4-Borono-trans-beta-nitrostyrene
  • trans-4-(beta-Nitrovinyl)phenylboronic acid
  • 4-[(E)-2-nitrovinyl]phenylboronic acid
  • {4-[(E)-2-nitroethenyl]phenyl}boronic acid
  • (E)-(4-(2-Nitrovinyl)phenyl)boronicacid
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