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CAS 380430-62-6

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(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid

Description:
(3-Benzyloxycarbonyl-5-nitrophenyl)boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a nitrophenyl group, which contributes to its electronic properties and potential reactivity, particularly in electrophilic aromatic substitution reactions. The benzyloxycarbonyl moiety enhances the compound's stability and solubility, making it suitable for various applications in organic synthesis and medicinal chemistry. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the nitro group can serve as a handle for further functionalization or as a site for reduction reactions. Overall, this compound is valuable in the development of pharmaceuticals and materials science due to its unique structural features and reactivity profile.
Formula:C14H12BNO6
InChI:InChI=1/C14H12BNO6/c17-14(22-9-10-4-2-1-3-5-10)11-6-12(15(18)19)8-13(7-11)16(20)21/h1-8,18-19H,9H2
SMILES:c1ccc(cc1)COC(=O)c1cc(cc(c1)N(=O)=O)B(O)O
Synonyms:
  • {3-[(Benzyloxy)Carbonyl]-5-Nitrophenyl}Boronic Acid
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