2-Heksanol

2-Heksanol
	Heksan-2-ol
Identifikacija
CAS registarski broj	626-93-7
PubChem	12297
ChemSpider	11794
ChEMBL	CHEMBL45425
Jmol-3D slike	Slika 1
SMILES
	OC(C)CCCC
InChI
	InChI=1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3 ; Kod: QNVRIHYSUZMSGM-UHFFFAOYSA-N InChI=1/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3; Kod: QNVRIHYSUZMSGM-UHFFFAOYAA
Svojstva
Molekulska formula	C6H14O
Molarna masa	102,174 g/mol
Gustina	0,81 g/mL
Tačka ključanja	140 °C, 413 K, 284 °F
Rastvorljivost u vodi	14 g/L
Rastvorljivost	rastvoran u etanolu, dietil etru
Termohemija
Standardna entalpija stvaranja jedinjenja ΔfHo298	-392,0 kJ·mol-1 (tečnost) ; -333,5 kJ·mol-1 (gas)
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

2-Heksanol (heksan-2-ol) je alkohol koji sadrži šest ugljenika. OH grupa je locirana na drugom atomu ugljeničnog lanca. Njegova hemijska formula je C₆H₁₄O ili C₆H₁₃OH. Postoji niz drugih strukturnih izomera. 2-Heksanol sadrži hiralni center, te modu razdvojiti dava enantiomera.

↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 3-310, 5-47, 8-106, ISBN 0-8493-0594-2
↑ 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
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[hand-1] Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 3-310, 5-47, 8-106, ISBN 0-8493-0594-2

[2] 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

[3] 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.

[4] 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

[5] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[1]

[2]

[3]

[4]

[5]