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CAS 568577-88-8

:

4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine

Description:
4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine, with the CAS number 568577-88-8, is an organic compound characterized by its complex structure that includes a morpholine ring and a boron-containing moiety. The presence of the dioxaborolane group suggests that it may exhibit unique reactivity, particularly in cross-coupling reactions, making it potentially useful in synthetic organic chemistry. The morpholine ring contributes to its solubility and may influence its biological activity, as morpholines are often found in pharmaceuticals. Additionally, the tetramethyl substitution on the dioxaborolane enhances its stability and steric hindrance, which can affect its reactivity and interactions with other molecules. This compound may be of interest in materials science and medicinal chemistry due to its potential applications in drug development and as a building block in organic synthesis. Overall, its unique structural features suggest a range of possible applications in various chemical contexts.
Formula:C16H24BNO3
InChI:InChI=1S/C16H24BNO3/c1-15(2)16(3,4)21-17(20-15)13-5-7-14(8-6-13)18-9-11-19-12-10-18/h5-8H,9-12H2,1-4H3
InChI key:InChIKey=UCPALIMHMYIZPZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC=C(C=C2)N3CCOCC3
Synonyms:
  • 4-(4-Morpholinyl)benzeneboronic acid pinacol ester
  • Morpholine, 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
  • N-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl]morpholine
  • 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine
  • 4-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine
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