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CAS 863753-35-9

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{2-[(tert-butoxycarbonyl)amino]pyridin-3-yl}boronic acid

Description:
{2-[(tert-butoxycarbonyl)amino]pyridin-3-yl}boronic acid is a boronic acid derivative characterized by the presence of a pyridine ring substituted with a tert-butoxycarbonyl (Boc) amino group. This compound typically exhibits properties associated with both boronic acids and amines, including 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. The presence of the Boc group provides protection for the amine functionality, allowing for selective reactions under specific conditions. Additionally, the boronic acid moiety can participate in Suzuki coupling reactions, which are valuable in the synthesis of complex organic molecules. The compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its reactivity and functional groups make it a versatile intermediate in medicinal chemistry and materials science. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C10H15BN2O4
InChI:InChI=1/C10H15BN2O4/c1-10(2,3)17-9(14)13-8-7(11(15)16)5-4-6-12-8/h4-6,15-16H,1-3H3,(H,12,13,14)
SMILES:CC(C)(C)OC(=Nc1c(cccn1)B(O)O)O
Synonyms:
  • 2-(tert-Butoxycarbonylamino)pyridine-3-boronicacid
  • 2-(tert-Butoxycarbonylamino)pyridine-3-boronic acid
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