Knowledge

1,2,3-Trinitrobenzene

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Parker, R. E.; Read, T. O. (1962). "The mechanism of displacement reactions. Part III. Kinetics of the reactions of the four 2-halogeno-1,3-dinitrobenzenes and 1,2,3-trinitrobenzene with aniline in ethanol".
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Except where otherwise noted, data are given for materials in their
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InChI=1S/C6H3N3O6/c10-7(11)4-2-1-3-5(8(12)13)6(4)9(14)15/h1-3H
208: 435: 170: 63: 455: 8: 462: 448: 223: 127: 15: 393:Journal of the Chemical Society (Resumed) 190: 382: 269: 244: 219: 251:Key: ONOWMDPHGJEBAZ-UHFFFAOYSA-N 107: 7: 416: 414: 161: 14: 418: 305: 299: 22: 339:(at 25 °C , 100 kPa). 311: 293: 1: 434:. You can help Knowledge by 502: 413: 272:c1cc(c(c(c1)(=O))(=O))(=O) 333: 280: 260: 235: 47: 35: 30: 21: 486:Aromatic compound stubs 426:This article about an 17:1,2,3-Trinitrobenzene 371:1,3,5-Trinitrobenzene 355:1,2,3-Trinitrobenzene 41:1,2,3-Trinitrobenzene 401:10.1039/JR9620003149 37:Preferred IUPAC name 329: g·mol 18: 343:Infobox references 16: 443: 442: 351:Chemical compound 349: 348: 204:CompTox Dashboard 89:Interactive image 493: 464: 457: 450: 422: 415: 405: 404: 387: 357:is an isomer of 328: 313: 307: 301: 295: 288:Chemical formula 228: 227: 212: 210: 194: 174: 163: 142: 131: 111: 91: 67: 26: 19: 501: 500: 496: 495: 494: 492: 491: 490: 471: 470: 469: 468: 411: 409: 408: 389: 388: 384: 379: 367: 359:trinitrobenzene 352: 345: 340: 326: 316: 310: 304: 298: 290: 276: 273: 268: 267: 256: 253: 252: 249: 243: 242: 231: 213: 206: 197: 177: 164: 152: 134: 114: 94: 81: 70: 57: 43: 42: 12: 11: 5: 499: 497: 489: 488: 483: 473: 472: 467: 466: 459: 452: 444: 441: 440: 430:compound is a 423: 407: 406: 381: 380: 378: 375: 374: 373: 366: 363: 350: 347: 346: 341: 337:standard state 334: 331: 330: 324: 318: 317: 314: 308: 302: 296: 291: 286: 283: 282: 278: 277: 275: 274: 271: 263: 262: 261: 258: 257: 255: 254: 250: 247: 246: 238: 237: 236: 233: 232: 230: 229: 221:DTXSID40209050 216: 214: 202: 199: 198: 196: 195: 187: 185: 179: 178: 176: 175: 167: 165: 157: 154: 153: 151: 150: 146: 144: 136: 135: 133: 132: 124: 122: 116: 115: 113: 112: 104: 102: 96: 95: 93: 92: 84: 82: 75: 72: 71: 69: 68: 60: 58: 53: 50: 49: 45: 44: 40: 39: 33: 32: 28: 27: 13: 10: 9: 6: 4: 3: 2: 498: 487: 484: 482: 481:Nitrobenzenes 479: 478: 476: 465: 460: 458: 453: 451: 446: 445: 439: 437: 433: 429: 424: 421: 417: 412: 402: 398: 394: 386: 383: 376: 372: 369: 368: 364: 362: 360: 356: 344: 338: 332: 325: 323: 320: 319: 292: 289: 285: 284: 279: 270: 266: 259: 245: 241: 234: 226: 222: 218: 217: 215: 205: 201: 200: 193: 189: 188: 186: 184: 181: 180: 173: 169: 168: 166: 160: 156: 155: 148: 147: 145: 143: 138: 137: 130: 126: 125: 123: 121: 118: 117: 110: 106: 105: 103: 101: 98: 97: 90: 86: 85: 83: 79: 74: 73: 66: 62: 61: 59: 56: 52: 51: 46: 38: 34: 29: 25: 20: 436:expanding it 425: 410: 392: 385: 354: 353: 48:Identifiers 281:Properties 109:CHEBI:48114 475:Categories 377:References 322:Molar mass 192:SPX6MW5XHL 120:ChemSpider 76:3D model ( 55:CAS Number 149:202-752-7 141:EC Number 428:aromatic 395:: 3149. 365:See also 65:603-13-4 327:213.105 159:PubChem 265:SMILES 172:521922 129:455276 31:Names 240:InChI 100:ChEBI 78:JSmol 432:stub 183:UNII 397:doi 209:EPA 162:CID 477:: 361:. 463:e 456:t 449:v 438:. 403:. 399:: 315:6 312:O 309:3 306:N 303:3 300:H 297:6 294:C 211:) 207:( 80:)

Index

Skeletal formula
Preferred IUPAC name
CAS Number
603-13-4
JSmol
Interactive image
ChEBI
CHEBI:48114
ChemSpider
455276
EC Number
PubChem
521922
UNII
SPX6MW5XHL
CompTox Dashboard
DTXSID40209050
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
trinitrobenzene
1,3,5-Trinitrobenzene
doi
10.1039/JR9620003149
Stub icon
aromatic

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