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CAS 850568-64-8

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2-(N-Boc-aminomethyl)-4-fluorophenylboronic acid

Description:
2-(N-Boc-aminomethyl)-4-fluorophenylboronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is substituted with a fluorine atom and an aminomethyl group protected by a Boc (tert-butyloxycarbonyl) 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 organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The Boc group serves as a protective group for the amine, allowing for selective reactions without interfering with the amine functionality. Additionally, the presence of the fluorine atom can influence the electronic properties and reactivity of the compound. Overall, this substance is valuable in medicinal chemistry and materials science for its potential applications in drug development and the synthesis of complex organic molecules.
Formula:C12H17BFNO4
InChI:InChI=1/C12H17BFNO4/c1-12(2,3)19-11(16)15-7-8-6-9(14)4-5-10(8)13(17)18/h4-6,17-18H,7H2,1-3H3,(H,15,16)
SMILES:CC(C)(C)OC(=NCc1cc(ccc1B(O)O)F)O
Synonyms:
  • (2-{[(tert-Butoxycarbonyl)amino]methyl}-4-fluorophenyl)boronic acid
  • carbamic acid, N-[(2-borono-5-fluorophenyl)methyl]-, 1,1-dimethylethyl ester
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