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CAS 1218789-33-3

:

N-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinamine

Description:
N-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinamine is a chemical compound characterized by its unique structural features, which include a pyrimidine ring and a cyclopropyl group. The presence of the dioxaborolane moiety suggests potential applications in medicinal chemistry, particularly in drug design, due to its ability to participate in various chemical reactions, including Suzuki coupling. This compound may exhibit specific biological activities, making it of interest in pharmaceutical research. Its molecular structure indicates potential for interactions with biological targets, possibly influencing enzyme activity or receptor binding. The cyclopropyl group can impart unique steric and electronic properties, which may enhance the compound's efficacy or selectivity. Additionally, the presence of boron in the dioxaborolane structure may contribute to its reactivity and stability under certain conditions. Overall, this compound represents a class of boron-containing heterocycles that are increasingly explored for their therapeutic potential and utility in organic synthesis.
Formula:C13H20BN3O2
InChI:InChI=1S/C13H20BN3O2/c1-12(2)13(3,4)19-14(18-12)9-7-15-11(16-8-9)17-10-5-6-10/h7-8,10H,5-6H2,1-4H3,(H,15,16,17)
InChI key:InChIKey=QNCUDGRKLRQDMW-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=NC(NC3CC3)=NC2
Synonyms:
  • N-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinamine
  • 2-Cyclopropylaminopyrimidine-5-boronic acid pinacol ester
  • 2-Pyrimidinamine, N-cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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