Date published: 2025-9-30

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4-Methoxystyrene (CAS 637-69-4)

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Alternate Names:
4-Vinylanisole
CAS Number:
637-69-4
Molecular Weight:
134.18
Molecular Formula:
C9H10O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Methoxystyrene (4-MS) is an aromatic hydrocarbon that has garnered extensive attention and exploration owing to its exceptional properties. This compound finds utility across diverse industries, including the production of plastics, coatings, and adhesives, as well as in the synthesis of specialty chemicals. Beyond its medical applications, 4-Methoxystyrene also plays a vital role in the production of specialty chemicals such as polymers, plastics, and coatings. The compound′s versatile nature and distinct properties contribute to its effectiveness in these industrial processes. Although the mechanism of action of 4-Methoxystyrene is not yet fully comprehended, ongoing research suggests that it interacts with specific proteins, notably the cytochrome P450 enzyme system. Furthermore, its interaction with DNA is believed to induce biochemical effects by inhibiting certain enzymes responsible for protein synthesis.


4-Methoxystyrene (CAS 637-69-4) References

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  2. Acyclic or long-bond intermediate in the electron-transfer-catalyzed dimerization of 4-methoxystyrene.  |  O'Neil, LL. and Wiest, O. 2006. J Org Chem. 71: 8926-33. PMID: 17081024
  3. Revealing shape selectivity and catalytic activity trends within the pores of H-ZSM-5 crystals by time- and space-resolved optical and fluorescence microspectroscopy.  |  Stavitski, E., et al. 2007. Chemistry. 13: 7057-65. PMID: 17639525
  4. Selectivity in the electron transfer catalyzed Diels-Alder reaction of (R)-alpha-phellandrene and 4-methoxystyrene.  |  Sevov, CS. and Wiest, O. 2008. J Org Chem. 73: 7909-15. PMID: 18785777
  5. A mechanistic investigation on copolymerization of ethylene with polar monomers using a cyclophane-based Pd(II) alpha-diimine catalyst.  |  Popeney, CS. and Guan, Z. 2009. J Am Chem Soc. 131: 12384-93. PMID: 19663488
  6. Evidence for behavioral attractiveness of methoxylated aromatics in a dynastid scarab beetle-pollinated araceae.  |  Dötterl, S., et al. 2012. J Chem Ecol. 38: 1539-43. PMID: 23143663
  7. Visible Light Photoinitiated Metal-Free Living Cationic Polymerization of 4-Methoxystyrene.  |  Perkowski, AJ., et al. 2015. J Am Chem Soc. 137: 7580-3. PMID: 26050662
  8. Mechanism of Oxygen Atom Transfer from Fe(V)(O) to Olefins at Room Temperature.  |  Singh, KK., et al. 2015. Inorg Chem. 54: 6112-21. PMID: 26053124
  9. Effects of volatile organic compounds from Streptomyces albulus NJZJSA2 on growth of two fungal pathogens.  |  Wu, Y., et al. 2015. J Basic Microbiol. 55: 1104-17. PMID: 26059065
  10. Characteristic Scent from the Tahitian Liverwort, Cyathodium foetidissimum.  |  Sakurai, K., et al. 2018. J Oleo Sci. 67: 1265-1269. PMID: 30305559
  11. Controlling the optical and catalytic properties of artificial metalloenzyme photocatalysts using chemogenetic engineering.  |  Zubi, YS., et al. 2022. Chem Sci. 13: 1459-1468. PMID: 35222930
  12. Integrating a fluorinated photoactive chromophore into metal-organic frameworks for selective trifluoroethylation of styrenes.  |  Hou, L., et al. 2023. Chem Commun (Camb). 59: 3407-3410. PMID: 36852572
  13. Droplet microreactor for high-throughput fluorescence-based measurements of single catalyst particle acidity.  |  Vollenbroek, JC., et al. 2023. Microsyst Nanoeng. 9: 39. PMID: 37007606

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Methoxystyrene, 5 g

sc-254697
5 g
$210.00

4-Methoxystyrene, 25 g

sc-254697A
25 g
$930.00