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CAS 627526-35-6

:

2-(4-Fluoro-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(4-Fluoro-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon framework. This compound is notable for its incorporation of a fluorinated naphthalene moiety, which can enhance its electronic properties and solubility in organic solvents. The presence of the tetramethyl groups contributes to its steric bulk, potentially influencing its reactivity and stability. Typically, compounds of this nature are utilized in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boron atom. The fluorine substituent may also impart specific electronic characteristics, making it useful in the development of materials or pharmaceuticals. Additionally, the compound's stability and solubility can be affected by the presence of the dioxaborolane ring, which can undergo hydrolysis under certain conditions. Overall, this compound exemplifies the versatility of organoboron chemistry in various applications, including medicinal chemistry and materials science.
Formula:C16H18BFO2
InChI:InChI=1S/C16H18BFO2/c1-15(2)16(3,4)20-17(19-15)13-9-10-14(18)12-8-6-5-7-11(12)13/h5-10H,1-4H3
InChI key:InChIKey=JYOPNVFIMNCXRZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C3=C(C(F)=CC2)C=CC=C3
Synonyms:
  • 2-(4-Fluoronaphthalen-1-yl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(4-fluoro-1-naphthalenyl)-4,4,5,5-tetramethyl-
  • 2-(4-Fluoro-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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