Date published: 2025-10-14

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2-Vinylanisole (CAS 612-15-7)

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CAS Number:
612-15-7
Molecular Weight:
134.18
Molecular Formula:
C9H10O
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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2-Vinylanisole applications span various industries. Extensive studies have explored the chemical and biological properties of 2-Vinylanisole, establishing it as useful in laboratory experiments. Scientific research has identified a wide range of applications for 2-Vinylanisole. It serves as a model compound for studying organic reaction mechanisms, acts as a substrate in enzymatic reactions, and functions as an enzyme inhibitor. Moreover, it has contributed to the exploration of protein structure and function. Notably, 2-Vinylanisole interacts with various enzymes, including cytochrome P450, carboxylesterases, and glutathione S-transferases. It also engages with proteins and other biological molecules such as DNA and RNA. The mechanism of action involves the binding of 2-VA to specific sites on enzymes or proteins, thereby inducing alterations in their structure and/or function. As research progresses, the multifaceted potential of 2-Vinylanisole continues to be unveiled, paving the way for future directions and discoveries in scientific investigations.


2-Vinylanisole (CAS 612-15-7) References

  1. Enantioselective synthesis of the AB-ring system of the antitumor antibiotic tetrazomine.  |  Wipf, P. and Hopkins, CR. 2001. J Org Chem. 66: 3133-9. PMID: 11325279
  2. Synthesis of pyrrolidines via palladium(II)-catalyzed aerobic oxidative carboamination of butyl vinyl ether and styrenes with allyl tosylamides.  |  Scarborough, CC. and Stahl, SS. 2006. Org Lett. 8: 3251-4. PMID: 16836378
  3. Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols.  |  Denmark, SE. and Butler, CR. 2008. J Am Chem Soc. 130: 3690-704. PMID: 18303892
  4. Detection of phenolic metabolites of styrene in mouse liver and lung microsomal incubations.  |  Shen, S., et al. 2010. Drug Metab Dispos. 38: 1934-43. PMID: 20724499
  5. Substituent Effects in the Surface-Initiated ATRP of Substituted Styrenes.  |  Saha, S. and Baker, GL. 2015. Appl Surf Sci. 359: 911-916. PMID: 26692601
  6. A Dual Palladium and Copper Hydride Catalyzed Approach for Alkyl-Aryl Cross-Coupling of Aryl Halides and Olefins.  |  Friis, SD., et al. 2017. Angew Chem Int Ed Engl. 56: 7242-7246. PMID: 28510287
  7. Investigation of the structural requirements for N-methyl-D-aspartate receptor positive and negative allosteric modulators based on 2-naphthoic acid.  |  Irvine, MW., et al. 2019. Eur J Med Chem. 164: 471-498. PMID: 30622023
  8. The Volatile Phytochemistry of Monarda Species Growing in South Alabama.  |  Lawson, SK., et al. 2021. Plants (Basel). 10: PMID: 33806521
  9. Elucidation of Analytical-Compositional Fingerprinting of Three Different Species of Chili Pepper by Using Headspace Solid-Phase Microextraction Coupled with Gas Chromatography-Mass Spectrometry Analysis, and Sensory Profile Evaluation.  |  Trovato, E., et al. 2022. Molecules. 27: PMID: 35408751
  10. Gymnosperms of Idaho: Chemical Compositions and Enantiomeric Distributions of Essential Oils of Abies lasiocarpa, Picea engelmannii, Pinus contorta, Pseudotsuga menziesii, and Thuja plicata.  |  Swor, K., et al. 2023. Molecules. 28: PMID: 36985451
  11. Dynamic Kinetic Resolution of 2-Phenylpropanal Derivatives to Yield β-Chiral Primary Amines via Bioamination  |   and Christine S. Fuchs, Manuel Hollauf, Maximilian Meissner, Robert C. Simon, Tatiana Besset, Joost N. H. Reek, Waander Riethorst, Ferdinand Zepeck, Wolfgang Kroutil. 2014. Advanced Synthesis & Catalysis. 356(10): 2257-2265.
  12. Stereoselective Synthesis of 1-Arylpropan-2-amines from Allylbenzenes through a Wacker-Tsuji Oxidation-Biotransamination Sequential Process  |   and Daniel González-Martínez, Vicente Gotor, Vicente Gotor-Fernández. 2019. Advanced Synthesis & Catalysis. 361(11): 2582-2593.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Vinylanisole, 1 g

sc-230691
1 g
$61.00