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CAS 883231-25-2

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[2-(tert-butoxycarbonylamino)pyrimidin-5-yl]boronic acid

Description:
[2-(tert-butoxycarbonylamino)pyrimidin-5-yl]boronic acid is a boronic acid derivative characterized by the presence of a pyrimidine ring substituted with a tert-butoxycarbonyl (Boc) amino group. This compound typically exhibits properties associated with both boronic acids and pyrimidine derivatives, including the ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug development and molecular recognition. The presence of the Boc group provides protection for the amino functionality, allowing for selective reactions in synthetic chemistry. Additionally, the boronic acid moiety can participate in Suzuki coupling reactions, making it valuable in organic synthesis for constructing carbon-carbon bonds. The compound is likely to be soluble in polar organic solvents, and its reactivity can be influenced by the pH of the environment due to the acidic nature of the boronic acid group. Overall, this substance is of interest in medicinal chemistry and materials science due to its unique structural features and reactivity.
Formula:C9H14BN3O4
InChI:InChI=1/C9H14BN3O4/c1-9(2,3)17-8(14)13-7-11-4-6(5-12-7)10(15)16/h4-5,15-16H,1-3H3,(H,11,12,13,14)
SMILES:CC(C)(C)OC(=Nc1ncc(cn1)B(O)O)O
Synonyms:
  • {2-[(tert-Butoxycarbonyl)amino]pyrimidin-5-yl}boronic acid
  • [2-[(tert-Butoxycarbonyl)amino]pyrimidin-5-yl]boronicacid
  • 2-(N-Boc-amino)pyrimidine-5-boronic acid
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