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CAS 287944-13-2

:

1,3,2-Dioxaborolane,2-(1-cyclohepten-1-yl)-4,4,5,5-tetramethyl-

Description:
1,3,2-Dioxaborolane, 2-(1-cyclohepten-1-yl)-4,4,5,5-tetramethyl- is an organoboron compound characterized by its dioxaborolane ring structure, which features a boron atom coordinated to two oxygen atoms and a carbon framework. This compound typically exhibits a cyclic structure that contributes to its stability and reactivity. The presence of the cycloheptene moiety introduces unsaturation, which can participate in various chemical reactions, including electrophilic additions and polymerization processes. The tetramethyl substitution enhances the steric bulk around the boron center, potentially influencing its reactivity and solubility in organic solvents. This compound may be utilized in organic synthesis, particularly in the formation of boron-containing intermediates or as a reagent in cross-coupling reactions. Its unique structural features make it a subject of interest in materials science and medicinal chemistry, where boron compounds are often explored for their biological activity and utility in drug development. Safety and handling precautions should be observed due to the potential reactivity of organoboron compounds.
Formula:C13H23BO2
Synonyms:
  • 1-Cyclohepten-1yl boronic acid pinacol ester
  • 1-Cycloheptenylboronic acid pinacol ester
  • 2-(Cyclohept-1-en-1-yl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(1-cyclohepten-1-yl)-4,4,5,5-tetramethyl-
  • 2-(cyclohepten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1-Cycloheptene-1-boronic Acid Pinacol Ester
  • (Z )-2-Cycloheptenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1-Cyclohepten-1-Boronic Acid Pinacol Ester
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