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CAS 218301-87-2

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4-N-Boc-amino-3-fluorophenylboronic acid

Description:
4-N-Boc-amino-3-fluorophenylboronic 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 applications, including medicinal chemistry and materials science. The "N-Boc" (tert-butoxycarbonyl) group serves as a protecting group for the amine, enhancing the compound's stability and facilitating its use in synthetic pathways. The presence of the fluorine atom on the phenyl ring can influence the compound's electronic properties and reactivity, potentially enhancing its biological activity. This compound is typically used in the synthesis of complex organic molecules and can participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the formation of carbon-carbon bonds. Its solubility and reactivity can vary depending on the solvent and reaction conditions, making it a versatile building block in organic synthesis. As with many boronic acids, it is important to handle this compound with care due to its potential reactivity and the need for proper storage conditions to maintain its integrity.
Formula:C11H15BFNO4
InChI:InChI=1/C11H15BFNO4/c1-11(2,3)18-10(15)14-9-5-4-7(12(16)17)6-8(9)13/h4-6,16-17H,1-3H3,(H,14,15)
SMILES:CC(C)(C)OC(=Nc1ccc(cc1F)B(O)O)O
Synonyms:
  • {4-[(tert-Butoxycarbonyl)amino]-3-fluorophenyl}boronic acid
  • Carbamic acid, N-(4-borono-2-fluorophenyl)-, 1,1-dimethylethyl ester
  • N-Boc-4-amino-3-fluorobenzeneboronic acid
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