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CAS 867333-29-7

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(2-chloro-5-nitro-phenyl)boronic acid

Description:
(2-Chloro-5-nitro-phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a chlorine atom and a nitro group. This compound typically appears as a solid and is soluble in polar organic solvents. Its structure features a boron atom bonded to a hydroxyl group and an aromatic ring, which enhances its reactivity in various chemical reactions, particularly in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. The presence of the nitro group introduces electron-withdrawing characteristics, which can influence the compound's reactivity and stability. Additionally, the chlorine substituent can participate in further substitution reactions. Due to its unique functional groups, (2-chloro-5-nitro-phenyl)boronic acid is of interest in medicinal chemistry and materials science, where it may serve as a building block for more complex molecules or as a reagent in the development of pharmaceuticals.
Formula:C6H5BClNO4
InChI:InChI=1/C6H5BClNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3,10-11H
SMILES:c1cc(c(cc1N(=O)=O)B(O)O)Cl
Synonyms:
  • (2-Chloro-5-nitrophenyl)boronic acid
  • boronic acid, B-(2-chloro-5-nitrophenyl)-
  • 2-Chloro-5-nitrophenylboronicacid
  • 2-Chloro-5-nitrophenylboronic acid
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