Molecular structure of 1-Nitro-4-vinylbenzene, CAS Number: 100-13-0
1-Nitro-4-vinylbenzene (CAS 100-13-0)
Alternate Names:
4-Nitrostyrene
CAS Number:
100-13-0
Purity:
≥95%
Molecular Weight:
149.15
Molecular Formula:
C8H7NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1-Nitro-4-vinylbenzene functions as a reactant in organic synthesis. Its mechanism of action involves participating in chemical reactions as a substrate, where it undergoes various transformations to yield different products. 1-Nitro-4-Vinylbenzene is involved in the formation of new carbon-carbon bonds and the introduction of functional groups, contributing to the diversification of chemical structures. At the molecular level, 1-Nitro-4-vinylbenzene interacts with other reagents to undergo addition reactions, leading to the formation of new chemical entities with distinct properties. Its involvement in these synthetic processes enables the generation of a wide range of compounds for further investigation and potential applications in various fields.
1-Nitro-4-vinylbenzene (CAS 100-13-0) References
- Copper/Silver Cocatalyzed Oxidative Coupling of Vinylarenes with ICH2CF3 or ICH2CHF2 Leading to β-CF3/CHF2-Substituted Ketones. | Yi, N., et al. 2016. Org Lett. 18: 1780-3. PMID: 27014795
- The synthesis of multi-substituted pyrrolidinones via a direct [3 + 2] cycloaddition of azaoxyallyl cations with aromatic ethylenes. | Zhang, Y., et al. 2018. Org Biomol Chem. 16: 4439-4442. PMID: 29855642
- Copper-Catalyzed Intermolecular Reductive Radical Difluoroalkylation-Thiolation of Aryl Alkenes. | Kong, W., et al. 2018. Org Lett. 20: 4975-4978. PMID: 30091931
- A versatile route to fabricate single atom catalysts with high chemoselectivity and regioselectivity in hydrogenation. | He, X., et al. 2019. Nat Commun. 10: 3663. PMID: 31413344
- An organoselenium-catalyzed N1- and N2-selective aza-Wacker reaction of alkenes with benzotriazoles. | Wang, X., et al. 2020. Chem Commun (Camb). 56: 4436-4439. PMID: 32195484
- Selectivity Reverse of Hydrosilylation of Aryl Alkenes Realized by Pyridine N-Oxide with [PSiP] Pincer Cobalt(III) Hydride as Catalyst. | Dong, Y., et al. 2021. Inorg Chem. 60: 4551-4562. PMID: 33677959
- Atomic engineering of single-atom nanozymes for enzyme-like catalysis. | Wu, W., et al. 2020. Chem Sci. 11: 9741-9756. PMID: 34094238
- OH−-induced β-elimination reactions with 1-(2-Xethyl)-4-nitrobenzene substrates in solvent mixture H 2 O/CH 3 CN and H 2 O/DMSO: Reactivity and mechanism | Alunni, S., Melis, R., & Ottavi, L. 2006. Research on chemical intermediates. 32: 827-836.
- Synthesis of 2-nitroso heterocyclic ketene aminals with (E)-1-nitro-4-(2-nitrovinyl)-benzene as the nitrosating agent | Yu, F. C., Hao, X. P., Huang, R., Yan, S. J., & Lin, J. 2015. Tetrahedron. 71(15): 2306-2312.
- Chloride-free and water-soluble Au complex for preparation of supported small nanoparticles by impregnation method | Murayama, H., Hasegawa, T., Yamamoto, Y., Tone, M., Kimura, M., Ishida, T.,.. & Tokunaga, M. 2017. Journal of Catalysis. 353: 74-80.
- Palladium-catalyzed four-component carbonylative synthesis of 2, 3-disubstituted quinazolin-4 (3H)-ones: Convenient methaqualone preparation | Peng, J. B., Geng, H. Q., Wang, W., Qi, X., Ying, J., & Wu, X. F. 2018. Journal of Catalysis. 365: 10-13.
- A visible-light responsive metal–organic framework as an eco-friendly photocatalyst under ambient air at room temperature | Liu, Y., Lin, C., Li, B., Wang, J., Wang, M., Zhang, N.,.. & Wu, P. 2020. Inorganic Chemistry Frontiers. 7(19): 3541-3547.
- Cobalt-catalyzed decarboxylative oxyalkylation of styrenes with α-cyanoacid: Access to γ‑ketonitriles | Chen, R., Wang, Y., Wang, Z. Y., Ma, X., Xu, C., Wang, K. K., & Sun, A. 2022. Tetrahedron Letters. 98: 153807.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Nitro-4-vinylbenzene, 1 mg | sc-297866 | 1 mg | $99.00 | |||
1-Nitro-4-vinylbenzene, 5 mg | sc-297866A | 5 mg | $84.00 | |||
1-Nitro-4-vinylbenzene, 1 g | sc-297866B | 1 g | $180.00 |