232:
139:
375:
24:
383:
355:
453:
653:
Arulsamy, N.; Bohle, D. S.; Butt, J. A.; Irvine, G. J.; Jordan, P. A.; Sagan, E. (1999). "Interrelationships between conformational dynamics and the redox chemistry of
271:
96:
449:
618:
246:
567:
445:
437:
488:
419:
189:
210:
374:
694:
146:
469:
465:
457:
134:
530:
The compound forms a number of unusual derivatives that are more stable than less bulky analogues. The
504:
397:
367:
36:
227:
62:
425:
433:
614:
547:
531:
601:
Garnsey, Michelle R.; Wengryniuk, Sarah E.; Coltart, Don M. (2009). "Triphenylmethanethiol".
666:
606:
294:
461:
198:
116:
689:
634:
Senning, Alexander (1991). "Triphenylmethanethiol and triphenylmethanesulfenyl chloride".
524:
441:
231:
138:
72:
482:
255:
InChI=1S/C19H16S/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H
683:
340:
127:
429:
178:
610:
473:
319:
107:
407:
165:
147:
670:
403:
481:
Except where otherwise noted, data are given for materials in their
520:
411:
95:
85:
23:
550:. It in turn reacts with ammonia to form the sulfenamide (C
215:
345:103–107 °C (217–225 °F; 376–380 K)
177:
566:. The thiol reacts with nitrous acid to give
71:
603:Encyclopedia of Reagents for Organic Synthesis
8:
230:
137:
115:
15:
279:C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)S
197:
659:Journal of the American Chemical Society
593:
276:
251:
226:
128:
546:CSCl is obtained from the thiol with
258:Key: JQZIKLPHXXBMCA-UHFFFAOYSA-N
7:
523:derivative of the bulky substituent
168:
14:
373:
306:
22:
485:(at 25 °C , 100 kPa).
312:
300:
1:
571:-nitrosotriphenylmethanethiol
711:
611:10.1002/047084289X.rn01030
479:
354:
349:
287:
267:
242:
55:
47:
35:
30:
21:
420:Precautionary statements
17:Triphenylmethanethiol
505:organosulfur compound
501:Triphenylmethanethiol
41:Triphenylmethanethiol
37:Preferred IUPAC name
507:with the formula (C
327: g·mol
18:
489:Infobox references
16:
671:10.1021/ja9901314
665:(30): 7115–7123.
657:-nitrosothiols".
548:sulfuryl chloride
532:sulfenyl chloride
527:(called trityl).
497:Chemical compound
495:
494:
398:Hazard statements
211:CompTox Dashboard
97:Interactive image
702:
695:Phenyl compounds
675:
674:
650:
644:
643:
631:
625:
624:
598:
519:CSH. It is the
475:
471:
467:
463:
459:
455:
451:
447:
443:
439:
435:
431:
427:
413:
409:
405:
377:
326:
314:
308:
302:
295:Chemical formula
235:
234:
219:
217:
201:
181:
170:
149:
141:
130:
119:
99:
75:
50:Trityl mercaptan
26:
19:
710:
709:
705:
704:
703:
701:
700:
699:
680:
679:
678:
652:
651:
647:
642:(4–5): 183–192.
633:
632:
628:
621:
600:
599:
595:
591:
584:
580:
576:
565:
561:
557:
553:
545:
541:
537:
525:triphenylmethyl
518:
514:
510:
498:
491:
486:
422:
400:
386:
370:
324:
311:
305:
297:
283:
280:
275:
274:
263:
260:
259:
256:
250:
249:
238:
220:
213:
204:
184:
171:
159:
122:
102:
89:
78:
65:
51:
43:
42:
12:
11:
5:
708:
706:
698:
697:
692:
682:
681:
677:
676:
645:
636:Sulfur Letters
626:
620:978-0471936237
619:
592:
590:
587:
582:
578:
574:
563:
559:
555:
551:
543:
539:
535:
516:
512:
508:
496:
493:
492:
487:
483:standard state
480:
477:
476:
454:P305+P351+P338
423:
418:
415:
414:
401:
396:
393:
392:
387:
382:
379:
378:
371:
366:
363:
362:
352:
351:
347:
346:
343:
337:
336:
333:
329:
328:
322:
316:
315:
309:
303:
298:
293:
290:
289:
285:
284:
282:
281:
278:
270:
269:
268:
265:
264:
262:
261:
257:
254:
253:
245:
244:
243:
240:
239:
237:
236:
223:
221:
209:
206:
205:
203:
202:
194:
192:
186:
185:
183:
182:
174:
172:
164:
161:
160:
158:
157:
153:
151:
143:
142:
132:
124:
123:
121:
120:
112:
110:
104:
103:
101:
100:
92:
90:
83:
80:
79:
77:
76:
68:
66:
61:
58:
57:
53:
52:
49:
45:
44:
40:
39:
33:
32:
28:
27:
13:
10:
9:
6:
4:
3:
2:
707:
696:
693:
691:
688:
687:
685:
672:
668:
664:
660:
656:
649:
646:
641:
637:
630:
627:
622:
616:
612:
608:
604:
597:
594:
588:
586:
572:
570:
549:
533:
528:
526:
522:
506:
502:
490:
484:
478:
424:
421:
417:
416:
402:
399:
395:
394:
391:
388:
385:
381:
380:
376:
372:
369:
365:
364:
360:
358:
353:
348:
344:
342:
341:Melting point
339:
338:
335:yellow solid
334:
331:
330:
323:
321:
318:
317:
299:
296:
292:
291:
286:
277:
273:
266:
252:
248:
241:
233:
229:
228:DTXSID1063142
225:
224:
222:
212:
208:
207:
200:
196:
195:
193:
191:
188:
187:
180:
176:
175:
173:
167:
163:
162:
155:
154:
152:
150:
145:
144:
140:
136:
133:
131:
129:ECHA InfoCard
126:
125:
118:
114:
113:
111:
109:
106:
105:
98:
94:
93:
91:
87:
82:
81:
74:
70:
69:
67:
64:
60:
59:
54:
46:
38:
34:
29:
25:
20:
662:
658:
654:
648:
639:
635:
629:
602:
596:
568:
529:
500:
499:
389:
356:
56:Identifiers
48:Other names
384:Signal word
332:Appearance
288:Properties
135:100.020.928
684:Categories
589:References
368:Pictograms
320:Molar mass
199:T7AQN86QSJ
108:ChemSpider
84:3D model (
63:CAS Number
470:P337+P313
466:P332+P313
450:P304+P340
446:P304+P312
442:P302+P352
359:labelling
156:223-020-3
148:EC Number
73:3695-77-0
350:Hazards
390:Warning
166:PubChem
690:Thiols
617:
585:CSNO.
503:is an
325:276.40
272:SMILES
31:Names
521:thiol
247:InChI
179:77281
117:69703
86:JSmol
615:ISBN
562:CSNH
474:P362
462:P321
458:P312
438:P280
434:P271
430:P264
426:P261
412:H332
408:H319
404:H315
190:UNII
667:doi
663:121
607:doi
357:GHS
216:EPA
169:CID
686::
661:.
640:12
638:.
613:.
605:.
573:(C
534:(C
472:,
468:,
464:,
460:,
456:,
452:,
448:,
444:,
440:,
436:,
432:,
428:,
410:,
406:,
361::
310:16
304:19
673:.
669::
655:S
623:.
609::
583:3
581:)
579:5
577:H
575:6
569:S
564:2
560:3
558:)
556:5
554:H
552:6
544:3
542:)
540:5
538:H
536:6
517:3
515:)
513:5
511:H
509:6
313:S
307:H
301:C
218:)
214:(
88:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
