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CAS 406463-06-7

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6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

Description:
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline, with the CAS number 406463-06-7, is a chemical compound that features a quinoline moiety substituted with a boron-containing group. This compound typically exhibits characteristics associated with both quinoline derivatives and boron compounds, such as potential applications in organic synthesis and medicinal chemistry. The presence of the dioxaborolane group suggests that it may participate in various chemical reactions, including Suzuki coupling, which is useful in forming carbon-carbon bonds. The tetramethyl substitution enhances its stability and solubility in organic solvents. Additionally, compounds like this may exhibit interesting photophysical properties, making them candidates for applications in materials science, such as in the development of organic light-emitting diodes (OLEDs) or as fluorescent probes. Overall, the unique structural features of this compound contribute to its versatility in synthetic and applied chemistry contexts.
Formula:C15H18BNO2
InChI:InChI=1/C15H18BNO2/c1-14(2)15(3,4)19-16(18-14)12-7-8-13-11(10-12)6-5-9-17-13/h5-10H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccc3c(cccn3)c2)O1
Synonyms:
  • 6-Quinolineboronic acid pinacol ester
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