1-Nitro-1-cyclohexene (CAS 2562-37-0)
QUICK LINKS
1-Nitro-1-cyclohexene functions as a reactive intermediate in organic synthesis. It interacts with cellular and molecular components by participating in various chemical reactions, particularly in the formation of other organic compounds. The mechanism of action of 1-Nitro-1-cyclohexene involves its ability to undergo addition reactions with nucleophiles, such as Grignard reagents or organolithium compounds, leading to the formation of new carbon-carbon bonds. 1-Nitro-1-cyclohexene can undergo reduction reactions to yield cyclohexanone derivatives, which can further participate in various cellular processes. 1-Nitro-1-cyclohexene can act as a dienophile in Diels-Alder reactions, enabling the formation of complex organic molecules. 1-Nitro-1-cyclohexene influences cellular processes or pathways by serving as a versatile building block for the synthesis of diverse organic compounds, thereby contributing to the molecular diversity and complexity of cellular systems.
1-Nitro-1-cyclohexene (CAS 2562-37-0) References
- Compounds that induce isoforms of glutathione S-transferase with properties of a critical enzyme in defense against oxidative stress. | Fiander, H. and Schneider, H. 1999. Biochem Biophys Res Commun. 262: 591-5. PMID: 10471368
- Dietary ortho phenols that induce glutathione S-transferase and increase the resistance of cells to hydrogen peroxide are potential cancer chemopreventives that act by two mechanisms: the alleviation of oxidative stress and the detoxification of mutagenic xenobiotics. | Fiander, H. and Schneider, H. 2000. Cancer Lett. 156: 117-24. PMID: 10880760
- Old yellow enzyme: stepwise reduction of nitro-olefins and catalysis of aci-nitro tautomerization. | Meah, Y. and Massey, V. 2000. Proc Natl Acad Sci U S A. 97: 10733-8. PMID: 10995477
- Palladium-catalyzed conjugate addition of organosiloxanes to alpha,beta-unsaturated carbonyl compounds and nitroalkenes. | Denmark, SE. and Amishiro, N. 2003. J Org Chem. 68: 6997-7003. PMID: 12946140
- Preparation of substituted anilines from nitro compounds by using supported gold catalysts. | Corma, A. and Serna, P. 2006. Nat Protoc. 1: 2590-5. PMID: 17406513
- Allylic C-H activations using Cu(II) 2-quinoxalinol salen and tert-butyl hydroperoxide. | Li, Y., et al. 2012. J Org Chem. 77: 4628-33. PMID: 22563758
- Redox Recycling Amplification Using an Interdigitated Microelectrode Array for Ionic Liquid-Based Oxygen Sensors. | Gondosiswanto, R., et al. 2018. Anal Chem. 90: 3950-3957. PMID: 29481063
- Identification of a common chemical signal regulating the induction of enzymes that protect against chemical carcinogenesis. | Talalay, P., et al. 1988. Proc Natl Acad Sci U S A. 85: 8261-5. PMID: 3141925
- Parallel induction of heme oxygenase-1 and chemoprotective phase 2 enzymes by electrophiles and antioxidants: regulation by upstream antioxidant-responsive elements (ARE). | Prestera, T., et al. 1995. Mol Med. 1: 827-37. PMID: 8612205
- In vitro anticancer activity of fruit extracts from Vaccinium species. | Bomser, J., et al. 1996. Planta Med. 62: 212-6. PMID: 8693031
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Nitro-1-cyclohexene, 5 g | sc-224771 | 5 g | $252.00 |