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CAS 69807-91-6

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1,3,2-Dioxaborolane,2-[3,5-bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl-

Description:
1,3,2-Dioxaborolane, 2-[3,5-bis(trifluoromethyl)phenyl]-4,4,5,5-tetramethyl- is a boron-containing heterocyclic compound characterized by its dioxaborolane ring structure, which features a five-membered cyclic arrangement containing two oxygen atoms and one boron atom. This compound is notable for its incorporation of a highly substituted phenyl group, specifically one that includes two trifluoromethyl groups, which significantly enhances its lipophilicity and alters its electronic properties. The presence of tetramethyl substituents contributes to steric hindrance, influencing its reactivity and stability. Typically, compounds of this nature are of interest in organic synthesis and materials science, particularly in the development of boron-based catalysts or ligands. The trifluoromethyl groups can impart unique characteristics, such as increased electron-withdrawing effects, which can affect the compound's behavior in chemical reactions. Overall, this compound exemplifies the intersection of organoboron chemistry and functionalized aromatic systems, making it a subject of interest in various chemical research applications.
Formula:C14H15BF6O2
InChI:InChI=1S/C14H15BF6O2/c1-11(2)12(3,4)23-15(22-11)10-6-8(13(16,17)18)5-9(7-10)14(19,20)21/h5-7H,1-4H3
InChI key:GGMXSSNJKVWXMD-UHFFFAOYSA-N
SMILES:B1(OC(C(O1)(C)C)(C)C)C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F
Synonyms:
  • 3,5-Bis(trifluoromethyl)phenylboronic acid pinacol ester
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