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CAS 871125-83-6

:

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

Description:
7-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline is a chemical compound characterized by its unique structure, which combines a quinoline moiety with a dioxaborolane group. The presence of the chlorine atom at the 7-position of the quinoline ring contributes to its reactivity and potential applications in medicinal chemistry. The dioxaborolane group, known for its stability and ability to form boron-containing compounds, enhances the compound's utility in various chemical reactions, particularly in cross-coupling reactions and as a potential building block in organic synthesis. This compound may exhibit interesting biological activities due to the quinoline scaffold, which is often associated with pharmacological properties. Additionally, the steric hindrance provided by the tetramethyl groups in the dioxaborolane can influence the compound's solubility and reactivity. Overall, 7-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline represents a versatile structure with potential applications in both synthetic and medicinal chemistry.
Formula:C15H17BClNO2
InChI:InChI=1S/C15H17BClNO2/c1-14(2)15(3,4)20-16(19-14)12-7-8-18-13-9-10(17)5-6-11(12)13/h5-9H,1-4H3
InChI key:InChIKey=GZDUYRAAWRRVEY-UHFFFAOYSA-N
SMILES:CC1(C)OB(C=2C3=C(C=C(Cl)C=C3)N=CC2)OC1(C)C
Synonyms:
  • (7-Chloroquinolin-4-yl)boronic acid pinacol ester
  • 7-Chloro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Quinoline
  • Quinoline, 7-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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