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CAS 5785-70-6

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(4-Ethoxycarbonyl-2-nitrophenyl)boronic acid

Description:
(4-Ethoxycarbonyl-2-nitrophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in organic synthesis and medicinal chemistry. The compound features a nitrophenyl group, which contributes to its electronic properties and reactivity, and an ethoxycarbonyl group that enhances its solubility and stability. Typically, boronic acids are utilized in Suzuki coupling reactions, allowing for the formation of carbon-carbon bonds, and they can also serve as intermediates in the synthesis of pharmaceuticals and agrochemicals. The presence of the nitro group can influence the acidity of the boronic acid, affecting its reactivity. Additionally, this compound may exhibit specific solubility characteristics in organic solvents and water, which can be important for its application in various chemical processes. Overall, (4-Ethoxycarbonyl-2-nitrophenyl)boronic acid is a versatile compound with significant utility in synthetic organic chemistry.
Formula:C18H14BrNO3
InChI:InChI=1/C18H14BrNO3/c1-20-15(11-7-9-13(19)10-8-11)14(17(22)18(20)23)16(21)12-5-3-2-4-6-12/h2-10,15,21H,1H3/b16-14+
Synonyms:
  • (4E)-5-(4-bromophenyl)-4-[hydroxy(phenyl)methylidene]-1-methylpyrrolidine-2,3-dione
  • 4-Ethoxycarbonyl-2-Nitrophenylboronic Acid
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