Date published: 2025-9-30

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Isopropenylboronic acid pinacol ester (CAS 126726-62-3)

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Application:
Isopropenylboronic acid pinacol ester is a substrate used in a palladium-catalyzed cross-coupling with olefins providing substituted 1,3-dienes
CAS Number:
126726-62-3
Molecular Weight:
168.04
Molecular Formula:
C9H17BO2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Isopropenylboronic acid pinacol ester functions as a versatile building block in organic synthesis. It acts as a key reagent in the formation of carbon-carbon and carbon-heteroatom bonds, playing a role in the construction of complex molecular structures. Through its mechanism of action, isopropenylboronic acid pinacol ester undergoes various chemical reactions, such as Suzuki-Miyaura cross-coupling, which enables the creation of new carbon-carbon bonds. Isopropenylboronic Acid Pinacol Ester also participates in palladium-catalyzed coupling reactions, facilitating the synthesis of diverse organic compounds. Isopropenylboronic acid pinacol ester can undergo oxidative addition and transmetalation processes, allowing for the incorporation of boron-containing fragments into organic molecules.


Isopropenylboronic acid pinacol ester (CAS 126726-62-3) References

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  7. Photocatalyzed regioselective hydrosilylation for the divergent synthesis of geminal and vicinal borosilanes.  |  Kong, D., et al. 2023. Nat Commun. 14: 2525. PMID: 37130840

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Isopropenylboronic acid pinacol ester, 5 g

sc-252922
5 g
$96.00