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CAS 169339-75-7

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TRANS-1-HEPTENYLBORONIC ACID PINACOL ESTER

Description:
Trans-1-heptenylylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boron atom bonded to a carbon chain with a double bond, specifically at the first position of a heptene. This compound typically features a pinacol ester functional group, which is derived from the reaction of boronic acids with pinacol, enhancing its stability and solubility in organic solvents. The trans configuration indicates that the substituents on the double bond are on opposite sides, which can influence its reactivity and physical properties. Generally, boronic acids and their esters are known for their utility in organic synthesis, particularly in cross-coupling reactions and as intermediates in the preparation of various organic compounds. The presence of the heptenyl group suggests potential applications in the synthesis of larger, more complex molecules. Additionally, this compound may exhibit specific reactivity patterns typical of boron-containing compounds, such as coordination with Lewis bases and participation in nucleophilic reactions. Safety data and handling precautions should be consulted due to the potential reactivity of organoboron compounds.
Formula:C13H25BO2
InChI:InChI=1/C13H25BO2/c1-6-7-8-9-10-11-14-15-12(2,3)13(4,5)16-14/h10-11H,6-9H2,1-5H3/b11-10+
Synonyms:
  • Trans-1-Heptenyl-1-Boronic Acid Pinacol Ester
  • Trans-4,4,5,5-Tetramethyl-2-Hept-1-Enyl-1,3,2-Dioxaborolane
  • E-2-(1-Heptenyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
  • 1-Heptenyl-1-Boronic Acid, Pinacol Ester
  • trans-1-Hepten-1-ylboronic acid pinacol ester, 97%
  • trans-1-Heptenylboronic acid pinacol ester, E-2-(1-Heptenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-[(1E)-hept-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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