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CAS 100960-11-0

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(2-Methyl-5-nitrophenyl)boronic acid

Description:
(2-Methyl-5-nitrophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a methyl group and a nitro group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the nitro group contributes to its electron-withdrawing properties, which can influence its reactivity and interactions in various chemical reactions, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Additionally, the boronic acid group allows for reversible binding with diols, making it useful in biological applications, such as in the development of sensors or drug delivery systems. Its unique structural features and functional properties make it a valuable compound in organic synthesis and materials science. Safety precautions should be observed when handling this compound, as with many organoboron compounds, due to potential toxicity and reactivity.
Formula:C7H8BNO4
InChI:InChI=1/C7H8BNO4/c1-5-2-3-6(9(12)13)4-7(5)8(10)11/h2-4,10-11H,1H3
SMILES:Cc1ccc(cc1B(O)O)N(=O)=O
Synonyms:
  • 2-Methyl-5-nitrophenylboronic acid
  • RARECHEM AH PB 0106
  • 5-Nitro-2-methylphenylboronic acid
  • 2-Methyl-5-nitrobenzeneboronic acid 96%
  • (2-METHYL-5-NITROPHENYL)BORONIC ACID
  • 2-METHYL-5-NITROBENZENEBORONIC ACID
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