Ciklohepten
Izgled
cis-Ciklohepten[1] | |||
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IUPAC ime |
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Drugi nazivi | cis-Ciklohepten | ||
Identifikacija | |||
CAS registarski broj | 628-92-2 | ||
PubChem[2][3] | 12363 | ||
ChemSpider[4] | 11857 | ||
Jmol-3D slike | Slika 1 | ||
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Svojstva | |||
Molekulska formula | C7H12 | ||
Molarna masa | 96.17 g/mol | ||
Gustina | 0.824 g/cm3 | ||
Tačka ključanja |
112-114.7 °C | ||
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |||
Infobox references |
Ciklohepten je sedmočlani cikloalken sa tačkom paljenja na -6 C°. On je gradivni materijal u organskoj hemiji i monomer u sintezi polimera. Ciklohepten može da postoji kao bilo cis- ili trans-izomer.[5][6]
- ↑ Cycloheptene
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.
- ↑ D. Cain, D. M. Pawar and E. A. Noe, "Conformational studies of trans-cycloheptene, trans-cycloheptene oxide, and trans-bicyclo [5.1.0] octane by ab initio calculations", Journal of Molecular Structure: THEOCHEM, volume 674, issues 1-3, April 2004, Pages 251-255
- ↑ Michael E. Squillacote, James DeFellipis, and Qingning Shu How Stable Is trans-Cycloheptene? J. Am. Chem. Soc.; 2005; 127(45) pp 15983 - 15988; (Article) DOI: 10.1021/ja055388i Abstract[mrtav link]