Ciklobuten

Ciklobuten
	Cyclobutene
Identifikacija
CAS registarski broj	822-35-5
PubChem	69972
ChemSpider	63164
EINECS broj	212-496-8
ChEBI	51206
Jmol-3D slike	Slika 1
SMILES
	C\1=C\CC/1
InChI
	InChI=1S/C4H6/c1-2-4-3-1/h1-2H,3-4H2 ; Kod: CFBGXYDUODCMNS-UHFFFAOYSA-N InChI=1/C4H6/c1-2-4-3-1/h1-2H,3-4H2; Kod: CFBGXYDUODCMNS-UHFFFAOYAN
Svojstva
Molekulska formula	C4H6
Molarna masa	54.09 g/mol
Gustina	0.733 g/cm3
Tačka ključanja	2 °C
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Ciklobuten je cikloalken. On se koristi u hemijskoj industriji kao monomer za sintezu polimera i za niz hemijskih sinteza.^[4]^[5]

Референце uredi

↑ 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. edit
↑ 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. edit
↑ Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
↑ Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th izd.). New York: Wiley-Interscience. ISBN 0-471-72091-7.

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