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CAS 85107-54-6

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(4-Carboxy-2-nitrophenyl)boronic acid

Description:
(4-Carboxy-2-nitrophenyl)boronic acid is an organic compound characterized by the presence of both a boronic acid functional group and a nitrophenyl moiety. It features a carboxylic acid group (-COOH) and a nitro group (-NO2) attached to a phenyl ring, which contributes to its acidic and electrophilic properties. The boronic acid group (-B(OH)2) allows for the formation of reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in chemical biology. This compound is typically a solid at room temperature and is soluble in polar solvents, such as water and alcohols, due to its polar functional groups. Its reactivity can be influenced by the presence of the nitro group, which can enhance electrophilicity and facilitate further chemical transformations. Overall, (4-Carboxy-2-nitrophenyl)boronic acid is a versatile compound with significant utility in medicinal chemistry and materials science.
Formula:C7H6BNO6
InChI:InChI=1/C7H6BNO6/c10-7(11)4-1-2-5(8(12)13)6(3-4)9(14)15/h1-3,12-13H,(H,10,11)
SMILES:c1cc(c(cc1C(=O)O)N(=O)=O)B(O)O
Synonyms:
  • 4-Borono-3-nitrobenzoic aci
  • 4-(Dihydroxyboranyl)-3-Nitrobenzoic Acid
  • 4-Carboxy-2-nitrophenylboronicacid
  • 4-Borono-3-Nitrobenzoic Acid
  • 4-Carboxy-2-Nitrophenylboronic Acid
  • 4-Carboxy-2-nitrobenzeneboronic acid
  • 4-Carboxy-2-nitrobenzeneboronic acid 97%
  • RARECHEM AH PB 0047
  • 4-CARBOXY-2-NITROPHENYLBORONIC ACID 97%
  • 4-Carboxy-2-Nitrophenylboronic
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