Knowledge (XXG)

Lucigenin

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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.
406: 442: 413: 170: 458: 23: 390:-methylacridinium nitrate. It exhibits a bluish-green fluorescence. 337:
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" 508: 397:
anion in biology, for its chemiluminescent properties.
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is an aromatic compound used in areas which include
182: 94: 528: 8: 535: 521: 215: 160: 138: 15: 433: 271: 236: 211: 151: 243:Key: KNJDBYZZKAZQNG-UHFFFAOYSA-N 7: 489: 487: 73:-Dimethyl-9,9'-bisacridinium nitrate 253:Key: KNJDBYZZKAZQNG-UHFFFAOYAH 173: 507:. You can help Knowledge (XXG) by 14: 491: 441:Amiet, R. Gary (February 1982). 345: 307: 301: 22: 341:(at 25 °C , 100 kPa). 313: 295: 1: 564:Quaternary ammonium compounds 447:Journal of Chemical Education 62:-methylacridinium nitrate; 386:. Its chemical name is bis- 585: 486: 412:There's also a route from 393:It is used as a probe for 335: 282: 262: 227: 78: 55: 35: 30: 21: 405:It may be prepared from 569:Aromatic compound stubs 499:This article about an 424: 422: 37:Preferred IUPAC name 331: g·mol 18: 425: 368:Infobox references 16: 516: 515: 459:10.1021/ed059p163 384:chemiluminescence 376:Chemical compound 374: 373: 196:CompTox Dashboard 120:Interactive image 576: 537: 530: 523: 495: 488: 478: 477: 475: 473: 438: 358: 352: 349: 348: 330: 315: 309: 303: 297: 290:Chemical formula 220: 219: 204: 202: 186: 175: 164: 153: 142: 122: 98: 71: 49:-diium dinitrate 48: 44: 26: 19: 584: 583: 579: 578: 577: 575: 574: 573: 544: 543: 542: 541: 484: 482: 481: 471: 469: 440: 439: 435: 430: 403: 377: 370: 365: 364: 363:  ?) 354: 350: 346: 342: 328: 318: 312: 306: 300: 292: 278: 275: 270: 269: 258: 255: 254: 251: 245: 244: 241: 235: 234: 223: 205: 198: 189: 176: 145: 125: 112: 101: 88: 74: 69: 51: 50: 46: 45:-Dimethyl-10,10 42: 12: 11: 5: 582: 580: 572: 571: 566: 561: 556: 546: 545: 540: 539: 532: 525: 517: 514: 513: 503:compound is a 496: 480: 479: 453:(2): 163–164. 432: 431: 429: 426: 402: 399: 375: 372: 371: 366: 344: 343: 339:standard state 336: 333: 332: 326: 320: 319: 316: 310: 304: 298: 293: 288: 285: 284: 280: 279: 277: 276: 273: 265: 264: 263: 260: 259: 257: 256: 252: 249: 248: 246: 242: 239: 238: 230: 229: 228: 225: 224: 222: 221: 213:DTXSID50177736 208: 206: 194: 191: 190: 188: 187: 179: 177: 169: 166: 165: 155: 147: 146: 144: 143: 135: 133: 127: 126: 124: 123: 115: 113: 106: 103: 102: 100: 99: 91: 89: 84: 81: 80: 76: 75: 57: 53: 52: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 581: 570: 567: 565: 562: 560: 557: 555: 552: 551: 549: 538: 533: 531: 526: 524: 519: 518: 512: 510: 506: 502: 497: 494: 490: 485: 468: 464: 460: 456: 452: 448: 444: 437: 434: 427: 421: 417: 415: 410: 408: 400: 398: 396: 391: 389: 385: 381: 369: 362: 357: 340: 334: 327: 325: 322: 321: 294: 291: 287: 286: 281: 272: 268: 261: 247: 237: 233: 226: 218: 214: 210: 209: 207: 197: 193: 192: 185: 181: 180: 178: 172: 168: 167: 163: 159: 156: 154: 152:ECHA InfoCard 149: 148: 141: 137: 136: 134: 132: 129: 128: 121: 117: 116: 114: 110: 105: 104: 97: 93: 92: 90: 87: 83: 82: 77: 72: 65: 61: 54: 38: 34: 29: 25: 20: 509:expanding it 498: 483: 470:. Retrieved 450: 446: 436: 411: 404: 392: 387: 379: 378: 79:Identifiers 67: 63: 59: 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 465:  356:verify 353:  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 409:. 201:EPA 174:CID 550:: 461:. 451:59 449:. 445:. 416:: 305:22 299:28 536:e 529:t 522:v 511:. 476:. 457:: 388:N 351:Y 317:6 314:O 311:4 308:N 302:H 296:C 203:) 199:( 111:) 70:′ 68:N 66:, 64:N 60:N 47:′ 43:′

Index


Preferred IUPAC name
CAS Number
2315-97-1
JSmol
Interactive image
ChemSpider
58609
ECHA InfoCard
100.017.295
Edit this at Wikidata
PubChem
65099
CompTox Dashboard
DTXSID50177736
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
verify
what is
Infobox references
chemiluminescence
superoxide
acridone
toluene
Synthesis of Lucigenin from Toluene. References in the image description.
"The preparation of lucigenin: An experiment with charm"

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