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CAS 1363386-57-5

:

4,4,5,5-Tetramethyl-2-[6-(2-methylpropoxy)-2-naphthalenyl]-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-[6-(2-methylpropoxy)-2-naphthalenyl]-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a naphthalene moiety. The presence of the dioxaborolane functional group suggests potential applications in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of boron in forming organoboron intermediates. The compound's bulky tetramethyl substituents enhance its steric properties, which can influence its reactivity and solubility in various solvents. Additionally, the 2-methylpropoxy group attached to the naphthalene ring may contribute to its hydrophobic characteristics, affecting its interaction with biological systems and materials. Overall, this compound's structural complexity and functional groups make it a candidate for research in fields such as medicinal chemistry, materials science, and catalysis. Its specific properties, such as melting point, boiling point, and solubility, would require experimental determination for practical applications.
Formula:C20H27BO3
InChI:InChI=1S/C20H27BO3/c1-14(2)13-22-18-10-8-15-11-17(9-7-16(15)12-18)21-23-19(3,4)20(5,6)24-21/h7-12,14H,13H2,1-6H3
InChI key:InChIKey=UEDXKTPSWIFJGL-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC3=C(C=C2)C=C(OCC(C)C)C=C3
Synonyms:
  • 2-(6-Isobutoxynaphthalen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[6-(2-methylpropoxy)-2-naphthalenyl]-
  • 4,4,5,5-Tetramethyl-2-[6-(2-methylpropoxy)-2-naphthalenyl]-1,3,2-dioxaborolane
  • 2-(6-Isobutoxy-naphthalen-2-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
  • 4,4,5,5-tetramethyl-2-[6-(2-methylpropoxy)naphthalen-2-yl]-1,3,2-dioxaborolane
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