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CAS 68716-52-9

:

4,4,5,5-tetramethyl-2-naphthalen-1-yl-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-naphthalen-1-yl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique structure, which includes a dioxaborolane ring fused with a naphthalene moiety. This compound typically exhibits a high degree of stability due to the presence of the boron atom, which can participate in various chemical reactions, particularly in cross-coupling reactions that are valuable in organic synthesis. The presence of the tetramethyl groups enhances its solubility in organic solvents and may influence its reactivity and steric properties. Additionally, the naphthalene structure contributes to its aromatic characteristics, which can affect its electronic properties and interactions with other molecules. This compound is often utilized in the synthesis of complex organic molecules and may serve as a precursor in the development of pharmaceuticals or materials science applications. Its specific reactivity and applications can vary based on the conditions under which it is used, making it a versatile compound in synthetic organic chemistry.
Formula:C16H19BO2
InChI:InChI=1/C16H19BO2/c1-15(2)16(3,4)19-17(18-15)14-11-7-9-12-8-5-6-10-13(12)14/h5-11H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cccc3ccccc23)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-naphthalenyl)-
  • 4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane
  • 1-Naphthylboronic acid pinacol ester
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