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CAS 865869-26-7

:

4,4,5,5-tetramethyl-2-(4-methylcyclohexen-1-yl)-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-(4-methylcyclohexen-1-yl)-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 typically exhibits a cyclic structure that contributes to its stability and reactivity. The presence of the 4-methylcyclohexen-1-yl group introduces a degree of unsaturation and steric hindrance, influencing its chemical behavior and potential applications in organic synthesis. Organoboron compounds like this one are often utilized in cross-coupling reactions, making them valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the presence of multiple methyl groups enhances its lipophilicity, which can affect solubility and reactivity in various solvents. Overall, this compound represents a versatile building block in synthetic organic chemistry, with potential applications in materials science and medicinal chemistry.
Formula:C13H23BO2
InChI:InChI=1/C13H23BO2/c1-10-6-8-11(9-7-10)14-15-12(2,3)13(4,5)16-14/h8,10H,6-7,9H2,1-5H3
SMILES:CC1CC=C(CC1)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • 4,4,5,5-TETRAMETHYL-2-(4-METHYLCYCLOHEX-1-ENYL)-1,3,2-DIOXABOROLANE
  • 4-Methyl-1-cyclohexene-1-boronic acid pinacol ester
  • 4,4,5,5-TetraMethyl-2-(4-Methyl-1-cyclohexen-1-yl)-1,3,2-dioxaborolane
  • 4,4,5,5-tetramethyl-2-(4-methylcyclohexen-1-yl)-1,3,2-dioxaborolane
  • 4-Methylcyclohexene-1-boronic Acid Pinacol Ester
  • 2-(4-Methyl-1-cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4,4,5,5-Tetramethyl-2-(4-methylcyclohex-1-enyl)-1,3,2-dioxaborolane (DDU to USA
  • 4-Methyl-1-cyclohexen-1-ylboronic acid pinacol ester
  • 4,4,5,5-TetraMethyl-2-(4-Methylcyclohex-1-en-1-yl)-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetraMethyl-2-(4-Methyl-1-cyclohexen-1-yl)-
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