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CAS 161395-96-6

:

E-2-(1-PENTENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE

Description:
E-2-(1-Pentenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, with CAS number 161395-96-6, is a boron-containing organic compound characterized by its unique dioxaborolane ring structure. This compound features a five-membered ring that includes two oxygen atoms and a boron atom, contributing to its stability and reactivity. The presence of the 1-pentenyl substituent introduces unsaturation, which can enhance its reactivity in various chemical transformations, particularly in organic synthesis and polymer chemistry. The four methyl groups attached to the dioxaborolane ring provide steric hindrance, influencing its physical properties such as boiling point and solubility. This compound is typically used as a reagent in organic synthesis, particularly in the formation of carbon-boron bonds, which are valuable in the development of pharmaceuticals and agrochemicals. Its specific reactivity and applications can vary based on the conditions and the presence of other functional groups in a reaction. Overall, this compound exemplifies the versatility of boron-containing compounds in modern chemistry.
Formula:C11H21BO2
InChI:InChI=1/C11H21BO2/c1-6-7-8-9-12-13-10(2,3)11(4,5)14-12/h8-9H,6-7H2,1-5H3/b9-8+
Synonyms:
  • 1-Pentenyl-1-Boronic Acid, Pinacol Ester
  • Trans-1-Pentenyl-1-Boronic Acid Pinacol Ester
  • Trans-1-Pentenylboronic Acid Pinacol Ester
  • Trans-4,4,5,5-Tetramethyl-2-Pent-1-Enyl-1,3,2-Dioxaborolane
  • trans-1-Penten-1-ylboronic acid pinacol ester
  • (E)-1-Pentenylboronic acid pinacol ester
  • trans-1-Pentenylboronic acid pinacol ester, E-2-(1-Pentenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4,4,5,5-tetramethyl-2-[(1E)-pent-1-en-1-yl]-1,3,2-dioxaborolane
  • (E)-4,4,5,5-tetramethyl-2-(pent-1-en-1-yl)-1,3,2-dioxaborolane
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