279:
204:
623:
41:
31:
57:
1144:
435:
431:
925:
513:
436:
434:
452:
526:
819:
701:
836:
Collins, Scott; Kelly, W. Mark (1992). "The microstructure of poly(cyclopentene) produced by polymerization of cyclopentene with homogeneous
Ziegler-Natta catalysts".
437:
604:
328:
579:. It has few applications, and thus is mainly used as a minor component of gasoline, present in concentrations of less than 1%. It is one of the principal
1185:
957:
871:
Sang, Rui; Kucmierczyk, Peter; Dühren, Ricarda; Razzaq, Rauf; Dong, Kaiwu; Liu, Jie; Franke, Robert; Jackstell, Ralf; Beller, Matthias (2019).
718:
459:
293:
40:
56:
1178:
533:
236:
648:
257:
1204:
950:
1171:
445:
30:
929:
611:
199:
1214:
634:
161:
943:
699:
Dieter Hönicke; Ringo Födisch; Peter Claus; Michael Olson (2002). "Cyclopentadiene and
Cyclopentene".
845:
69:
1068:
1063:
274:
87:
1080:
1053:
1048:
902:
644:
622:
1209:
1126:
1121:
894:
796:
714:
549:
1155:
121:
1105:
884:
853:
788:
761:
706:
351:
734:
245:
1040:
779:
Baldwin, John E. (2003). "Thermal
Rearrangements of Vinylcyclopropanes to Cyclopentenes".
615:
491:
181:
97:
1143:
849:
278:
203:
141:
1075:
1035:
592:
504:
1198:
906:
600:
402:
392:
192:
1002:
982:
225:
1151:
1017:
1012:
1007:
997:
987:
966:
580:
495:
471:
735:"Hydrocarbon Composition of Gasoline Vapor Emissions from Enclosed Fuel Tanks"
372:
172:
765:
710:
640:
898:
889:
873:"Synthesis of Carboxylic Acids by Palladium‐Catalyzed Hydroxycarbonylation"
872:
800:
924:
458:
451:
444:
417:
857:
1100:
596:
382:
212:
792:
1092:
974:
572:
568:
152:
503:
Except where otherwise noted, data are given for materials in their
1027:
132:
120:
110:
576:
939:
935:
637:
yields 1,3-linkages, not the more typical 1,2-linked polymer.
262:
39:
29:
752:
B. B. Corson, V. N. Ipatieff (1939). "Cyclohexylbenzene".
591:
Cyclopentene is produced industrially in large amounts by
429:
407:
44 to 46 °C (111 to 115 °F; 317 to 319 K)
1159:
521:
741:. United States Environmental Protection Agency. 2011.
599:. In the laboratory, it is prepared by dehydration of
603:. Substituted cyclopentenes are the product of the
1114:
1091:
1026:
973:
224:
433:
96:
702:Ullmann's Encyclopedia of Industrial Chemistry
1179:
951:
8:
820:Ullmanns Enzyklopädie der Technischen Chemie
813:D. Hönicke, R. Födisch, P. Claus, M. Olson:
605:vinylcyclopropane-cyclopentene rearrangement
1186:
1172:
958:
944:
936:
277:
202:
180:
18:
16:Organic compound; 5-sided hydrocarbon ring
888:
244:
677:
673:
669:
665:
661:
657:
563:
559:
555:
397:−135 °C (−211 °F; 138 K)
363:
359:
877:Angewandte Chemie International Edition
691:
333:
298:
273:
633:The polymerization of cyclopentene by
476:−29 °C (−20 °F; 244 K)
302:InChI=1S/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2
193:
312:InChI=1/C5H8/c1-2-4-5-3-1/h1-2H,3-5H2
305:Key: LPIQUOYDBNQMRZ-UHFFFAOYSA-N
160:
140:
7:
1140:
1138:
44:Ball-and-stick model of cyclopentene
315:Key: LPIQUOYDBNQMRZ-UHFFFAOYAS
215:
1158:. You can help Knowledge (XXG) by
14:
1142:
923:
815:Cyclopentadiene and Cyclopentene
621:
511:
55:
610:It can also be produced by the
507:(at 25 °C , 100 kPa).
1:
649:cyclopentanecarboxylic acid
25:
1231:
1137:
501:
480:
411:
377:68.11 g/mol
344:
324:
289:
80:
68:
63:
54:
24:
766:10.15227/orgsyn.019.0036
711:10.1002/14356007.a08_227
705:. Weinheim: Wiley-VCH.
635:Ziegler-Natta catalysts
612:catalytic hydrogenation
890:10.1002/anie.201908451
826:, Wiley-VCH, Weinheim.
647:of cyclopentene gives
440:
45:
35:
1150:This article about a
439:
43:
33:
932:at Wikimedia Commons
567:. It is a colorless
422:(fire diamond)
70:Preferred IUPAC name
1069:1,4-Cycloheptadiene
1064:1,3-Cycloheptadiene
883:(40): 14365–14373.
858:10.1021/ma00027a039
850:1992MaMol..25..233C
21:
1081:1,5-Cyclooctadiene
1054:1,4-Cyclohexadiene
1049:1,3-Cyclohexadiene
645:hydrocarboxylation
534:Infobox references
481:Related compounds
441:
46:
36:
19:
1205:Hydrocarbon stubs
1167:
1166:
1135:
1134:
1127:Cyclononatetraene
1122:Cyclooctatetraene
928:Media related to
793:10.1021/cr010020z
754:Organic Syntheses
552:with the formula
550:chemical compound
542:Chemical compound
540:
539:
487:Related compounds
258:CompTox Dashboard
122:Interactive image
50:
49:
1222:
1188:
1181:
1174:
1146:
1139:
1106:Cycloheptatriene
1060:Cycloheptadiene
960:
953:
946:
937:
927:
911:
910:
892:
868:
862:
861:
833:
827:
811:
805:
804:
781:Chemical Reviews
776:
770:
769:
749:
743:
742:
731:
725:
724:
696:
681:
625:
566:
524:
518:
515:
514:
461:
454:
447:
432:
366:
352:Chemical formula
282:
281:
266:
264:
248:
228:
217:
206:
195:
184:
164:
144:
124:
100:
59:
26:
22:
1230:
1229:
1225:
1224:
1223:
1221:
1220:
1219:
1195:
1194:
1193:
1192:
1136:
1131:
1110:
1087:
1045:Cyclohexadiene
1041:Cyclopentadiene
1022:
969:
964:
920:
915:
914:
870:
869:
865:
835:
834:
830:
812:
808:
787:(4): 1197–212.
778:
777:
773:
751:
750:
746:
733:
732:
728:
721:
698:
697:
693:
688:
679:
675:
671:
667:
663:
659:
655:
631:
616:cyclopentadiene
589:
565:
561:
557:
553:
543:
536:
531:
530:
529: ?)
520:
516:
512:
508:
494:
492:Cyclopentadiene
488:
466:
465:
464:
463:
456:
449:
442:
438:
430:
365:
361:
357:
354:
340:
337:
332:
331:
320:
317:
316:
313:
307:
306:
303:
297:
296:
285:
267:
260:
251:
231:
218:
187:
167:
147:
127:
114:
103:
90:
76:
75:
17:
12:
11:
5:
1228:
1226:
1218:
1217:
1212:
1207:
1197:
1196:
1191:
1190:
1183:
1176:
1168:
1165:
1164:
1147:
1133:
1132:
1130:
1129:
1124:
1118:
1116:
1112:
1111:
1109:
1108:
1103:
1097:
1095:
1089:
1088:
1086:
1085:
1084:
1083:
1076:Cyclooctadiene
1073:
1072:
1071:
1066:
1058:
1057:
1056:
1051:
1043:
1038:
1036:Cyclobutadiene
1032:
1030:
1024:
1023:
1021:
1020:
1015:
1010:
1005:
1000:
995:
990:
985:
979:
977:
971:
970:
965:
963:
962:
955:
948:
940:
934:
933:
919:
918:External links
916:
913:
912:
863:
838:Macromolecules
828:
806:
771:
744:
726:
720:978-3527306732
719:
690:
689:
687:
684:
683:
682:
630:
627:
593:steam cracking
588:
585:
541:
538:
537:
532:
510:
509:
505:standard state
502:
499:
498:
489:
486:
483:
482:
478:
477:
474:
468:
467:
457:
450:
443:
428:
427:
426:
425:
423:
414:
413:
409:
408:
405:
399:
398:
395:
389:
388:
385:
379:
378:
375:
369:
368:
355:
350:
347:
346:
342:
341:
339:
338:
335:
327:
326:
325:
322:
321:
319:
318:
314:
311:
310:
308:
304:
301:
300:
292:
291:
290:
287:
286:
284:
283:
270:
268:
256:
253:
252:
250:
249:
241:
239:
233:
232:
230:
229:
221:
219:
211:
208:
207:
197:
189:
188:
186:
185:
177:
175:
169:
168:
166:
165:
157:
155:
149:
148:
146:
145:
137:
135:
129:
128:
126:
125:
117:
115:
108:
105:
104:
102:
101:
93:
91:
86:
83:
82:
78:
77:
73:
72:
66:
65:
61:
60:
52:
51:
48:
47:
37:
15:
13:
10:
9:
6:
4:
3:
2:
1227:
1216:
1215:Cyclopentenes
1213:
1211:
1208:
1206:
1203:
1202:
1200:
1189:
1184:
1182:
1177:
1175:
1170:
1169:
1163:
1161:
1157:
1153:
1148:
1145:
1141:
1128:
1125:
1123:
1120:
1119:
1117:
1113:
1107:
1104:
1102:
1099:
1098:
1096:
1094:
1090:
1082:
1079:
1078:
1077:
1074:
1070:
1067:
1065:
1062:
1061:
1059:
1055:
1052:
1050:
1047:
1046:
1044:
1042:
1039:
1037:
1034:
1033:
1031:
1029:
1025:
1019:
1016:
1014:
1011:
1009:
1006:
1004:
1001:
999:
996:
994:
991:
989:
986:
984:
981:
980:
978:
976:
972:
968:
961:
956:
954:
949:
947:
942:
941:
938:
931:
926:
922:
921:
917:
908:
904:
900:
896:
891:
886:
882:
878:
874:
867:
864:
859:
855:
851:
847:
843:
839:
832:
829:
825:
822:
821:
816:
810:
807:
802:
798:
794:
790:
786:
782:
775:
772:
767:
763:
759:
755:
748:
745:
740:
739:nepis.epa.gov
736:
730:
727:
722:
716:
712:
708:
704:
703:
695:
692:
685:
654:
653:
652:
650:
646:
642:
638:
636:
628:
626:
624:
619:
617:
613:
608:
606:
602:
601:cyclopentanol
598:
594:
586:
584:
582:
578:
574:
570:
551:
547:
535:
528:
523:
506:
500:
497:
493:
490:
485:
484:
479:
475:
473:
470:
469:
462:
455:
448:
424:
421:
420:
416:
415:
410:
406:
404:
403:Boiling point
401:
400:
396:
394:
393:Melting point
391:
390:
386:
384:
381:
380:
376:
374:
371:
370:
356:
353:
349:
348:
343:
334:
330:
323:
309:
299:
295:
288:
280:
276:
275:DTXSID6029171
272:
271:
269:
259:
255:
254:
247:
243:
242:
240:
238:
235:
234:
227:
223:
222:
220:
214:
210:
209:
205:
201:
198:
196:
194:ECHA InfoCard
191:
190:
183:
179:
178:
176:
174:
171:
170:
163:
162:ChEMBL1797299
159:
158:
156:
154:
151:
150:
143:
139:
138:
136:
134:
131:
130:
123:
119:
118:
116:
112:
107:
106:
99:
95:
94:
92:
89:
85:
84:
79:
71:
67:
62:
58:
53:
42:
38:
32:
28:
27:
23:
20:Cyclopentene
1160:expanding it
1149:
1003:Cycloheptene
993:Cyclopentene
992:
983:Cyclopropene
967:Cycloalkenes
930:Cyclopentene
880:
876:
866:
844:(1): 233–7.
841:
837:
831:
823:
818:
814:
809:
784:
780:
774:
757:
753:
747:
738:
729:
700:
694:
639:
632:
620:
609:
590:
581:cycloalkenes
546:Cyclopentene
545:
544:
418:
81:Identifiers
74:Cyclopentene
34:Cyclopentene
1152:hydrocarbon
1018:Cyclodecene
1013:Cyclononene
1008:Cyclooctene
998:Cyclohexene
988:Cyclobutene
664:+ CO + H
643:-catalyzed
496:Cyclobutene
472:Flash point
387:0.771 g/cm
345:Properties
200:100.005.030
142:CHEBI:49155
1199:Categories
686:References
587:Production
373:Molar mass
246:ONM2CKV81Z
173:ChemSpider
109:3D model (
88:CAS Number
1115:Tetraenes
907:199466915
668:O → C
641:Palladium
629:Reactions
1210:Monomers
899:31390131
801:12683781
419:NFPA 704
412:Hazards
336:C1CC=CC1
98:142-29-0
1101:Benzene
1093:Trienes
975:Alkenes
846:Bibcode
597:naphtha
571:with a
527:what is
525: (
383:Density
367:
213:PubChem
1028:Dienes
905:
897:
817:, in:
799:
760:: 36.
717:
575:-like
573:petrol
569:liquid
522:verify
519:
329:SMILES
153:ChEMBL
64:Names
1154:is a
903:S2CID
548:is a
294:InChI
133:ChEBI
111:JSmol
1156:stub
895:PMID
824:2002
797:PMID
715:ISBN
577:odor
562:(CH)
237:UNII
226:8882
182:8544
885:doi
854:doi
789:doi
785:103
762:doi
707:doi
614:of
595:of
554:(CH
263:EPA
216:CID
1201::
901:.
893:.
881:58
879:.
875:.
852:.
842:25
840:.
795:.
783:.
758:19
756:.
737:.
713:.
676:CO
651::
618:.
607:.
583:.
1187:e
1180:t
1173:v
1162:.
959:e
952:t
945:v
909:.
887::
860:.
856::
848::
803:.
791::
768:.
764::
723:.
709::
680:H
678:2
674:9
672:H
670:5
666:2
662:8
660:H
658:5
656:C
564:2
560:3
558:)
556:2
517:N
460:1
453:3
446:1
364:8
362:H
360:5
358:C
265:)
261:(
113:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
