Date published: 2026-2-15

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2-Bromostyrene (CAS 2039-88-5)

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Alternate Names:
o -Bromovinylbenzene
CAS Number:
2039-88-5
Molecular Weight:
183.05
Molecular Formula:
C8H7Br
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-Bromostyrene is a chemical compound that functions as a substrate in organic synthesis reactions. It participates in various cross-coupling reactions to form carbon-carbon bonds, such as Suzuki-Miyaura and Heck reactions. In these processes, 2-Bromostyrene acts as an electrophile, undergoing nucleophilic substitution or oxidative addition with other reagents to form new carbon-carbon bonds. 2-Bromostyrene′s mode of action involves its ability to undergo halogen-metal exchange reactions, enabling the introduction of diverse functional groups into organic molecules. 2-Bromostyrene can serve as a starting material for the synthesis of various organic compounds, contributing to the development of new materials and chemical entities. Its role in organic synthesis allows for the construction of complex molecular structures and the modification of existing compounds, supporting the advancement of chemical research and development.


2-Bromostyrene (CAS 2039-88-5) References

  1. Synthesis of heterocycles via Pd-ligand controlled cyclization of 2-chloro-N-(2-vinyl)aniline: preparation of carbazoles, indoles, dibenzazepines, and acridines.  |  Tsvelikhovsky, D. and Buchwald, SL. 2010. J Am Chem Soc. 132: 14048-51. PMID: 20858012
  2. Mechanistic studies of copper(I)-catalyzed 1,3-halogen migration.  |  Van Hoveln, R., et al. 2015. J Am Chem Soc. 137: 5346-54. PMID: 25828031
  3. Formal Asymmetric Hydrobromination of Styrenes via Copper-Catalyzed 1,3-Halogen Migration.  |  Van Hoveln, RJ., et al. 2014. Chem Sci. 5: 4763-4767. PMID: 26167268
  4. Bioinspired Synthesis of a Sedaxane Metabolite Using Catalytic Vanadyl Acetylacetonate and Molecular Oxygen.  |  Tyagi, S., et al. 2015. J Org Chem. 80: 11941-7. PMID: 26619065
  5. Synthesis of Phthalans Via Copper-Catalyzed Enantioselective Cyclization/Carboetherification of 2-Vinylbenzyl Alcohols.  |  Chen, D. and Chemler, SR. 2018. Org Lett. 20: 6453-6456. PMID: 30336677
  6. Comprehensive GC×GC-qMS with a mass-to-charge ratio difference extraction method to identify new brominated byproducts during ozonation and their toxicity assessment.  |  Zhang, XY., et al. 2021. J Hazard Mater. 403: 124103. PMID: 33265069
  7. Interrupted Intramolecular Hydroaminomethylation of N-Protected-2-vinyl Anilines: Novel Access to 3-Substitued Indoles or Indoline-2-ols.  |  Hochberger-Roa, F., et al. 2022. Molecules. 27: PMID: 35164340
  8. Characteristics of the formation and toxicity index of nine newly identified brominated disinfection byproducts during wastewater ozonation.  |  Zhang, XY., et al. 2022. Sci Total Environ. 824: 153924. PMID: 35182650
  9. Crucial Factors Regulating Intramolecular Charge-Transfer-Based Radiative Efficiency in ortho-Carboranyl Luminophores: Planarity between Substituted Biphenyl Rings.  |  Kim, M., et al. 2022. ACS Omega. 7: 24027-24039. PMID: 35847313
  10. Research Progress of the Endocrine-Disrupting Effects of Disinfection Byproducts.  |  Sui, S., et al. 2022. J Xenobiot. 12: 145-157. PMID: 35893263
  11. Enantiospecific Syntheses of Congested Atropisomers through Chiral Bis(aryne) Synthetic Equivalents.  |  Dauvergne, G., et al. 2022. Chemistry. 28: e202202473. PMID: 35943888
  12. Diverse Synthesis of Alkenylsilanes via Pd-Catalyzed Alkenyl C-H Silylation.  |  Ye, ZH., et al. 2023. Org Lett. 25: 2145-2150. PMID: 36921249
  13. Strategies in the synthesis of dibenzo[b,f]heteropines.  |  Maier, DIH., et al. 2023. Beilstein J Org Chem. 19: 700-718. PMID: 37284586

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromostyrene, 1 g

sc-251717
1 g
$55.00

2-Bromostyrene, 5 g

sc-251717A
5 g
$139.00