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CAS 1356165-79-1

:

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,5-naphthyridine

Description:
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,5-naphthyridine is a chemical compound characterized by its unique structural features, which include a naphthyridine moiety and a boron-containing dioxaborolane group. The presence of the dioxaborolane ring contributes to its potential reactivity, particularly in cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The compound is likely to exhibit moderate to high lipophilicity due to the naphthyridine structure, which may influence its biological activity and solubility in organic solvents. Additionally, the tetramethyl substitution on the dioxaborolane enhances its stability and steric hindrance, potentially affecting its reactivity and interactions with other molecules. As with many boron-containing compounds, it may also participate in Lewis acid-base chemistry. Overall, this compound's characteristics make it a subject of interest for researchers in fields such as drug development and materials science.
Formula:C14H17BN2O2
InChI:InChI=1S/C14H17BN2O2/c1-13(2)14(3,4)19-15(18-13)10-8-12-11(17-9-10)6-5-7-16-12/h5-9H,1-4H3
InChI key:InChIKey=ZLJJTKKBVUARJC-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC3=C(N=C2)C=CC=N3
Synonyms:
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,5-naphthyridine
  • 1,5-Naphthyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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