| Company Name: |
BePharm Ltd |
| Tel: |
400-685-9117 |
| Email: |
market@bepharm.com |
9-(2-nitrovinyl)anthracene manufacturers
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| | 9-(2-nitrovinyl)anthracene Basic information |
| Product Name: | 9-(2-nitrovinyl)anthracene | | Synonyms: | 9-(2-nitrovinyl)anthracene;9-(2-Nitroethenyl)anthracene;Einecs 261-220-2;(E)-9-(2-Nitrovinyl)anthracene;Anthracene,9-(2-nitroethenyl)- | | CAS: | 58349-77-2 | | MF: | C16H11NO2 | | MW: | 249.26 | | EINECS: | 261-220-2 | | Product Categories: | | | Mol File: | 58349-77-2.mol |  |
| | 9-(2-nitrovinyl)anthracene Chemical Properties |
| | 9-(2-nitrovinyl)anthracene Usage And Synthesis |
| Synthesis | GENERAL METHOD: 9-Anthracenecarboxaldehyde (1; 2.06 g, 10 mmol) was dissolved in anhydrous dichloromethane (20 mL). To this solution nitromethane (559 μL, 10 mmol) and piperidine (202 μL, 2 mmol) were added sequentially. The reaction mixture was heated to reflux and maintained for 8 hours. After completion of the reaction, it was cooled to room temperature and a red solid precipitated. The solid product was collected by filtration and washed with hexane (20 mL) to afford the target compound 9-(2-nitrovinyl)anthracene (1.70 g, 68% yield) as a red solid. Compound Registry Number: 55446-60-1; Thin Layer Chromatography Rf value = 0.56 (Expanding Agent Ratio: Hexane:Ethyl Acetate = 80:20); 1H NMR (CDCl3, 300 MHz) δ = 7.49-7.65 (m, 5H, aromatic hydrogens and -CH=CHNO2), 8.07 (d, J=7.9 Hz, 2H, aromatic hydrogens), 8.20 (d, J=8.8 Hz, 2H, aromatic hydrogen), 8.56 (s, 1H, H-10), 9.03 (d, J=13.8 Hz, 1H, -CH=CHNO2). Ref: Becker, H.D.; Soerensen, H.; Sandros, K. J. Org. Chem. 1986, 51, 3223-3226. | | References | [1] Tetrahedron Letters, 2013, vol. 54, # 32, p. 4306 - 4308 [2] Doklady Chemistry, 1975, vol. 225, p. 681 - 684 [3] Dokl. Akad. Nauk SSSR Ser. Khim., 1975, vol. 225, # 6, p. 1323 - 1326 [4] Inorganica Chimica Acta, 2015, vol. 426, p. 119 - 125 [5] Synthetic Communications, 2017, vol. 47, # 6, p. 551 - 556 |
| | 9-(2-nitrovinyl)anthracene Preparation Products And Raw materials |
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