Date published: 2025-10-21

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1-Propenylmagnesium bromide solution (CAS 14092-04-7)

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Application:
CAS Number:
14092-04-7
Molecular Weight:
145.28
Molecular Formula:
C3H5BrMg
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.
Available in US only.
* Refer to Certificate of Analysis for lot specific data.

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1-Propenylmagnesium bromide solution stands as a prominent organometallic compound that has found widespread use in the realm of organic synthesis. Its significance lies in its role as a versatile reagent for crafting an array of organic compounds, including alcohols, ketones, and carboxylic acids. Organic synthesis has greatly benefited from the extensive utilization of 1-Propenylmagnesium bromide solution, particularly in the creation of alcohols, ketones, and carboxylic acids. As a valuable reagent, it facilitates the establishment of carbon-carbon bonds and the introduction of essential functional groups. 1-Propenylmagnesium bromide solution operates as a potent nucleophile, effectively targeting electrophilic carbon atoms within organic compounds. The ensuing reaction generally follows the SN2 mechanism, where the magnesium atom assumes the role of a Lewis acid, thereby stabilizing the negative charge on the carbon atom. The result is the formation of a carbon-magnesium bond, which can subsequently engage in further reactions with diverse electrophiles.


1-Propenylmagnesium bromide solution (CAS 14092-04-7) References

  1. Gold(I)-catalyzed formation of bicyclo[4.2.0]oct-1-enes.  |  Felix, RJ., et al. 2013. J Org Chem. 78: 5685-90. PMID: 23663099
  2. Synthesis of Carbazoles and Carbazole-Containing Heterocycles via Rhodium-Catalyzed Tandem Carbonylative Benzannulations.  |  Song, W., et al. 2016. J Org Chem. 81: 2930-42. PMID: 26963834
  3. Characterization of typical potent odorants in raw and cooked Toona sinensis (A. Juss.) M. Roem. by instrumental-sensory analysis techniques.  |  Yang, W., et al. 2019. Food Chem. 282: 153-163. PMID: 30711100
  4. Sulfamate-Tethered Aza-Wacker Cyclization Strategy for the Syntheses of 2-Amino-2-deoxyhexoses: Preparation of Orthogonally Protected d-Galactosamines.  |  Paul, D., et al. 2023. J Org Chem. 88: 1445-1456. PMID: 36649480

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Propenylmagnesium bromide solution, 100 ml

sc-222738
100 ml
$116.00
US: Only available in the US

1-Propenylmagnesium bromide solution, 800 ml

sc-222738A
800 ml
$466.00
US: Only available in the US