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CAS 736990-42-4

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2-(3-Fluorophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2-(3-Fluorophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, identified by its CAS number 736990-42-4, is an organic compound featuring a pyridine ring substituted with a 3-fluorophenyl group and a boron-containing moiety. The presence of the fluorophenyl group introduces electron-withdrawing characteristics, which can influence the compound's reactivity and interaction with other molecules. The dioxaborolane unit contributes to the compound's potential as a boron source, making it useful in various synthetic applications, particularly in organic synthesis and medicinal chemistry. This compound may exhibit unique solubility properties due to its polar and nonpolar regions, affecting its behavior in different solvents. Additionally, the steric bulk provided by the tetramethyl groups can impact the compound's stability and reactivity. Overall, this compound's structure suggests potential applications in drug development, materials science, and as a building block in the synthesis of more complex organic molecules.
Formula:C17H19BFNO2
InChI:InChI=1S/C17H19BFNO2/c1-16(2)17(3,4)22-18(21-16)13-8-9-20-15(11-13)12-6-5-7-14(19)10-12/h5-11H,1-4H3
InChI key:InChIKey=UQOUANLGYSOGCK-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(N=CC2)C3=CC(F)=CC=C3
Synonyms:
  • 2-(3-Fluorophenyl) pyridine-4-boronic acid pinacol ester
  • Pyridine, 2-(3-fluorophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-(3-Fluorophenyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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