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Chlorotrifluoroethylene

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Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2002). "Fluorine Compounds, Organic".
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The thermal dimerization of chlorotrifluoroethylene gives 1,2-dichloro-1,2,3,3,4,4-hexafluorocyclobutane. Dechlorination of the latter gives
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Buxton, M. W.; Ingram, D. W.; Smith, F.; Stacey, M.; Tatlow, J. C. (1952). "The High-Temperature Dimerisation of Chlorotrifluoroethylene".
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In 2012, an estimated 1–10 million pounds were produced commercially in the United States.
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R. E. Putnam, B. C. Anderson, W. H. Sharkey (1963). "1-Chloro-1,4,4-Trifluorobutadiene".
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Chlorotrifluoroethylene is produced commercially by the dechlorination of
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in Japan, and it used to be produced under the trade name Kel-F from
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Except where otherwise noted, data are given for materials in their
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Aetna Plastics Corp. - Products. Services ... Solutions
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in cryogenic applications. CTFE has a carbon-carbon
1135: 581: 205: 849:. PCTFE has the trade name Neoflon PCTFE from 686: 99: 48:Ball-and-stick model of chlorotrifluoroethylene 979:Ullmann's Encyclopedia of Industrial Chemistry 655: 585: 433:−158.2 °C (−252.8 °F; 115.0 K) 1118: 38:Structural formula of chlorotrifluoroethylene 1060:: CS1 maint: multiple names: authors list ( 443:−27.8 °C (−18.0 °F; 245.3 K) 860: 16:"CTFE" redirects here. For other uses, see 1144:Heating, ventilation, and air conditioning 1125: 1111: 635: 284: 165: 143: 1013:Journal of the Chemical Society (Resumed) 241: 845:or copolymerized to produce the plastic 280: 1136: 156: 867:1,1,2-trichloro-1,2,2-trifluoroethane 312:Key: UUAGAQFQZIEFAH-UHFFFAOYSA-N 1077: 923: 917: 322:Key: UUAGAQFQZIEFAH-UHFFFAOYAH 196: 13: 969: 903:. It undergoes cycloaddition to 682: 43: 33: 14: 1180: 926:Handbook of Chemistry and Physics 1081: 780: 543: 538: 533: 373: 370: 776:(at 25 °C , 100 kPa). 1027: 1004: 942: 364: 69:1-Chloro-1,2,2-trifluoroethene 1: 910: 825:with chemical formula CFCl=CF 1097:. You can help Knowledge by 309:InChI=1S/C2ClF3/c3-1(4)2(5)6 7: 843:polychlorotrifluoroethylene 829:. It is commonly used as a 319:InChI=1/C2ClF3/c3-1(4)2(5)6 29: 10: 1185: 1076: 15: 770: 733: 514: 509: 423:1.54 g/cm at −60°C 351: 331: 296: 83: 75: 63: 58: 28: 1048:10.15227/orgsyn.043.0017 988:10.1002/14356007.a11_349 861:Production and reactions 757:Dichlorodifluoroethylene 594:Precautionary statements 24:Chlorotrifluoroethylene 982:. Weinheim: Wiley-VCH. 924:Lide, David R. (1998). 815:Chlorotrifluoroethylene 761:Trichlorofluoroethylene 479:Magnetic susceptibility 1089:This article about an 749:Bromotrifluoroethylene 693: 49: 39: 901:hexafluorocyclobutene 885:Cl + Zn → CClF=CF 753:Trifluoroiodoethylene 692: 78:Chlorotrifluoroethene 47: 37: 18:CTFE (disambiguation) 1021:10.1039/JR9520003830 675:(fire diamond) 65:Preferred IUPAC name 958:on 27 November 2022 765:Tetrachloroethylene 745:Tetrafluoroethylene 450:Solubility in water 391: g·mol 25: 1169:Organohalide stubs 823:chlorofluorocarbon 803:Infobox references 734:Related compounds 694: 50: 40: 23: 1106: 1105: 1036:Organic Syntheses 851:Daikin Industries 811:Chemical compound 809: 808: 740:Related compounds 568:Hazard statements 265:CompTox Dashboard 125:Interactive image 54: 53: 1176: 1127: 1120: 1113: 1085: 1078: 1066: 1065: 1059: 1051: 1031: 1025: 1024: 1008: 1002: 1001: 973: 967: 966: 965: 963: 946: 940: 939: 921: 793: 787: 784: 783: 725:Explosive limits 714: 707: 700: 685: 665: 661: 657: 653: 649: 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point 437: 436: 432: 430: 429:Melting point 427: 426: 422: 420: 417: 416: 412: 408: 406: 403: 402: 398: 395: 394: 387: 385: 382: 381: 363: 360: 356: 355: 350: 341: 340: 337: 330: 316: 306: 305: 302: 295: 287: 283: 282:DTXSID3026485 279: 278: 276: 266: 262: 261: 257: 255: 252: 251: 244: 240: 239: 237: 235: 232: 231: 224: 223: 221: 219: 216: 215: 208: 204: 203: 201: 195: 191: 190: 183: 182: 180: 178: 173: 172: 168: 164: 161: 159: 157:ECHA InfoCard 154: 153: 146: 142: 141: 139: 137: 134: 133: 126: 122: 121: 119: 115: 110: 109: 102: 98: 97: 95: 92: 88: 87: 82: 74: 66: 62: 57: 46: 42: 36: 32: 31: 27: 19: 1154:Refrigerants 1099:expanding it 1088: 1073: 1071: 1056:cite journal 1039: 1035: 1029: 1012: 1006: 977: 971: 960:, retrieved 956:the original 950: 944: 925: 919: 898: 895: 864: 818: 814: 813: 671: 559: 516: 505:1.38 (0 °C) 495: 218:RTECS number 84:Identifiers 76:Other names 1159:Haloalkenes 839:polymerized 835:double bond 831:refrigerant 554:Signal word 465:soluble in 396:Appearance 352:Properties 163:100.001.093 1138:Categories 962:3 February 911:References 528:Pictograms 471:chloroform 461:Solubility 384:Molar mass 243:AF215GW34G 136:ChemSpider 112:3D model ( 91:CAS Number 729:24-40.3% 660:P410+P403 652:P403+P233 624:P304+P340 620:P301+P310 519:labelling 254:UN number 225:KV0525000 184:201-201-8 176:EC Number 1015:: 3830. 841:to form 672:NFPA 704 510:Hazards 481:(χ) 889:+ ZnCl 821:) is a 796:what is 794: ( 467:benzene 419:Density 411:etheral 194:PubChem 101:79-38-9 1042:: 17. 994:  932:  791:verify 788:  560:Danger 409:faint 389:116.47 336:SMILES 59:Names 1093:is a 869:with 847:ECTFE 413:odor 301:InChI 258:1082 114:JSmol 1095:stub 1062:link 992:ISBN 964:2012 930:ISBN 877:CFCl 871:zinc 819:CTFE 664:P501 656:P405 648:P403 644:P381 640:P377 636:P330 632:P321 628:P311 616:P271 612:P270 608:P264 604:P261 600:P210 586:H331 582:H301 578:H280 574:H220 405:Odor 234:UNII 207:6594 145:6345 1044:doi 1017:doi 984:doi 881:-CF 517:GHS 270:EPA 197:CID 1140:: 1058:}} 1054:{{ 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Index

CTFE (disambiguation)
Structural formula of chlorotrifluoroethylene
Ball-and-stick model of chlorotrifluoroethylene
Preferred IUPAC name
CAS Number
79-38-9
JSmol
Interactive image
ChemSpider
6345
ECHA InfoCard
100.001.093
Edit this at Wikidata
EC Number
PubChem
6594
RTECS number
UNII
AF215GW34G
UN number
CompTox Dashboard
DTXSID3026485
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
Odor
etheral
Density

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