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CAS 1072945-60-8

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2-Methyl-3-Nitrophenylboronic Acid

Description:
2-Methyl-3-Nitrophenylboronic Acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methyl and a nitro substituent. This compound typically exhibits a white to off-white crystalline appearance. It is soluble in polar solvents such as water and alcohols, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The presence of the nitro group introduces electron-withdrawing characteristics, influencing the compound's reactivity and making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. Additionally, the boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it valuable in the development of sensors and drug delivery systems. Its applications extend to medicinal chemistry, where it may serve as a building block for pharmaceuticals. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.
Formula:C7H8BNO4
InChI:InChI=1S/C7H8BNO4/c1-5-6(8(10)11)3-2-4-7(5)9(12)13/h2-4,10-11H,1H3
SMILES:Cc1c(cccc1N(=O)=O)B(O)O
Synonyms:
  • (2-Methyl-3-nitrophenyl)boronic acid
  • 2-METHYL-3-NITROPHENYLBORONIC ACID
  • 2-METHYL-3-NITROBENZENEBORONIC ACID
  • Boronic acid, B-(2-methyl-3-nitrophenyl)-
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