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InChI=1S/C28H22N2.2NO3/c1-29-23-15-7-3-11-19(23)27(20-12-4-8-16-24(20)29)28-21-13-5-9-17-25(21)30(2)26-18-10-6-14-22(26)28;2*2-1(3)4/h3-18H,1-2H3;;/q+2;2*-1
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InChI=1/C28H22N2.2NO3/c1-29-23-15-7-3-11-19(23)27(20-12-4-8-16-24(20)29)28-21-13-5-9-17-25(21)30(2)26-18-10-6-14-22(26)28;2*2-1(3)4/h3-18H,1-2H3;;/q+2;2*-1
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Synthesis of
Lucigenin from Toluene. References in the image description.
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390:-methylacridinium nitrate. It exhibits a bluish-green fluorescence.
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Except where otherwise noted, data are given for materials in their
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C1c2ccccc2c(c3c1cccc3)c4c5ccccc5(c6c4cccc6)C.(=O)().(=O)()
443:"The preparation of lucigenin: An experiment with charm"
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anion in biology, for its chemiluminescent properties.
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is an aromatic compound used in areas which include
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243:Key: KNJDBYZZKAZQNG-UHFFFAOYSA-N
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73:-Dimethyl-9,9'-bisacridinium nitrate
253:Key: KNJDBYZZKAZQNG-UHFFFAOYAH
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507:. You can help Knowledge (XXG) by
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441:Amiet, R. Gary (February 1982).
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341:(at 25 °C , 100 kPa).
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564:Quaternary ammonium compounds
447:Journal of Chemical Education
62:-methylacridinium nitrate;
386:. Its chemical name is bis-
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412:There's also a route from
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37:Preferred IUPAC name
331: g·mol
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368:Infobox references
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459:10.1021/ed059p163
384:chemiluminescence
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120:Interactive image
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49:-diium dinitrate
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509:expanding it
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79:Identifiers
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56:Other names
472:20 November
283:Properties
158:100.017.295
548:Categories
428:References
395:superoxide
324:Molar mass
131:ChemSpider
107:3D model (
86:CAS Number
17:Lucigenin
559:Acridines
467:0021-9584
401:Synthesis
380:Lucigenin
96:2315-97-1
554:Nitrates
501:aromatic
407:acridone
414:toluene
361:what is
359: (
329:510.506
171:PubChem
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356:verify
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267:SMILES
31:Names
232:InChI
184:65099
140:58609
109:JSmol
41:10,10
505:stub
474:2023
463:ISSN
58:Bis-
455:doi
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201:EPA
174:CID
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388:N
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317:6
314:O
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308:N
302:H
296:C
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68:N
66:,
64:N
60:N
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43:′
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