Date published: 2026-4-4

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2-Bromobenzaldehyde ethylene acetal (CAS 34824-58-3)

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Alternate Names:
2-Bromobenzaldehyde ethylene acetal
CAS Number:
34824-58-3
Molecular Weight:
229.07
Molecular Formula:
C9H9BrO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Bromobenzaldehyde ethylene acetal, also referred to as 2-(2-Bromophenyl)-1,3-dioxolane or 2-bromo-1,3-dioxolane, belongs to the dioxolane family, a class of heterocyclic compounds. This colorless and volatile liquid possesses a pungent odor and a low melting point. Its significance lies in its role as a intermediate in the synthesis of pharmaceuticals, agrochemicals, and various organic compounds. In the realm of scientific research, 2-Bromobenzaldehyde ethylene aceta has found widespread use across multiple applications. It serves as a building block in the synthesis of polymers, dyes, and catalysts. Moreover, it plays a pivotal role in the synthesis of agrochemicals. Its versatility extends to enabling the creation of various other compounds, including polymers, dyes, and catalysts. When employed in organic synthesis and polymer synthesis 2-Bromobenzaldehyde ethylene aceta acts as a nucleophile, targeting the electrophilic center of the substrate and establishing a covalent bond. Additionally, it also acts as a catalyst, expediting the reaction rate and facilitating the formation of desired products. 2-Bromobenzaldehyde ethylene aceta holds significant importance as a versatile compound, playing key roles in various industries and scientific research endeavors, making it an essential component in the synthesis of diverse products.


2-Bromobenzaldehyde ethylene acetal (CAS 34824-58-3) References

  1. Phosphino hydrazones as suitable ligands in the asymmetric Suzuki-Miyaura cross-coupling.  |  Ros, A., et al. 2012. J Org Chem. 77: 4740-50. PMID: 22510026
  2. Asymmetric Allylation/RCM-Mediated Synthesis of Fluorinated Benzo-Fused Bicyclic Homoallylic Amines As Dihydronaphthalene Derivatives.  |  Sedgwick, DM., et al. 2016. J Org Chem. 81: 8876-8887. PMID: 27574907
  3. Thermal and photochemical reactions of syn-oxabenzosesquinorbornene (1,2,3,4,9,10-hexahydro-9,10-exo-epoxy-1,4-exo-methanoanthracene)  |  Paul D. Bartlett and Gerald L. Combs Jr. 1984. J. Org. Chem., 49, 4,: 625–630.
  4. Tandem Processes in C-Aryl Ketenes and Ketenimines Triggered by [1,5]-Hydride-Like Migration of an Acetalic Hydrogen Atom  |   and Angel Vidal, Marta Marin-Luna, Mateo Alajarin. February 2014. European Journal of Organic Chemistry. Volume2014, Issue4: Pages 878-886.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromobenzaldehyde ethylene acetal, 5 g

sc-230065
5 g
$57.00