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CAS 871332-90-0

:

[3-(benzylcarbamoyl)-5-nitro-phenyl]boronic acid

Description:
[3-(Benzylcarbamoyl)-5-nitro-phenyl]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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a nitro group and a benzylcarbamoyl moiety, contributing to its potential biological activity and reactivity. Its structure suggests it may participate in Suzuki coupling reactions, a common method for forming carbon-carbon bonds in organic synthesis. The presence of the nitro group can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. Additionally, the boronic acid group can act as a ligand in coordination chemistry. This compound may also exhibit interesting pharmacological properties, making it a candidate for further research in drug development. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C14H13BN2O5
InChI:InChI=1/C14H13BN2O5/c18-14(16-9-10-4-2-1-3-5-10)11-6-12(15(19)20)8-13(7-11)17(21)22/h1-8,19-20H,9H2,(H,16,18)
SMILES:c1ccc(cc1)CN=C(c1cc(cc(c1)N(=O)=O)B(O)O)O
Synonyms:
  • [3-(Benzylcarbamoyl)-5-nitrophenyl]boronic acid
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