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CAS 874219-56-4

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

Description:
[3-(Benzyloxycarbonylamino)-5-nitro-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a nitro group and a benzyloxycarbonylamino group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The nitro group contributes to its electron-withdrawing characteristics, potentially influencing its reactivity and solubility in different solvents. The benzyloxycarbonylamino moiety enhances its stability and can facilitate interactions with biological targets. Overall, this compound is of interest in the development of pharmaceuticals and as a building block in organic synthesis due to its unique structural features and functional groups. Its specific reactivity and applications would depend on the context of its use in chemical reactions or biological systems.
Formula:C14H13BN2O6
InChI:InChI=1/C14H13BN2O6/c18-14(23-9-10-4-2-1-3-5-10)16-12-6-11(15(19)20)7-13(8-12)17(21)22/h1-8,19-20H,9H2,(H,16,18)
SMILES:c1ccc(cc1)COC(=Nc1cc(cc(c1)N(=O)=O)B(O)O)O
Synonyms:
  • (3-{[(Benzyloxy)carbonyl]amino}-5-nitrophenyl)boronic acid
  • 3-Amino-5-nitrobenzeneboronicacid,CBZprotected98%
  • N-CBZ-3-AMINO-5-NITROBENZENEBORONIC ACID
  • 3-AMINO-5-NITROBENZENEBORONIC ACID, CBZ PROTECTED
  • 3-(Benzyloxycarbonylamino)-5-nitrobenzeneboronic acid
  • 3-Amino-5-nitrobenzeneboronic acid, CBZ protected 98%
  • 3-(Benzyloxycarbonylamino)-5-nitrophenylboronic
  • Benzyl (3-borono-5-nitro)phenylcarbamate
  • 3-(BENZYLOXYCARBONYLAMINO)-5-NITROPHENYLBORONIC ACID
  • Carbamic acid, (3-borono-5-nitrophenyl)-, C-(phenylmethyl) ester (9CI)
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