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Naftohinon
	4a,8a-Dihidronaftalen-1,4-dion
Drugi nazivi	1α-Naftohinon
Identifikacija
CAS registarski broj	130-15-4
PubChem	8530
ChemSpider	8215
ChEMBL	CHEMBL55934
Jmol-3D slike	Slika 1
SMILES
	O=C2C=CC(C1=CC=CC=C12)=O
InChI
	InChI=1S/C10H6O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H ; Kod: FRASJONUBLZVQX-UHFFFAOYSA-N InChI=1/C10H6O2/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H; Kod: FRASJONUBLZVQX-UHFFFAOYAK
Svojstva
Molekulska formula	C10H6O2
Molarna masa	158,15 g/mol
Gustina	1,422 g/cm3
Tačka topljenja	126 °C
Tačka ključanja	Počinje da sublimira na 100 °C
Rastvorljivost u vodi	0,09 g/L
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1,4-Naftohinon je organsko jedinjenje izvedeno iz naftalina. Nekoliko izomernih naftohinona je poznato, npr. 1,2-naftohinon. 1,4-Naftohinon formira isparljive žute triklinične kristale i ima oštar miris sličan benzohinonu. On je skoro potpuno nerastvoran u hladnoj vodi, malo rastvoran u petrolejskom etru, i u većoj meri u polarnim organskim rastvaračima. U alkalinnim rastvorima on proizvodi crvenkasto-smeđu boju. Vitamin K je derivat 1,4-naftohinona. On je planaran molekul sa romatičnim prstenom kondenzovanim sa hinonskom jedinicom.^[6]

Reference

↑ Merck Index, 11th Edition, 6315.
↑ 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
↑ Gaultier, J.; Hauw, C. (1965). „Structure de l'α-Naphtoquinone”. Acta Crystallographica 18 (2): 179–183. DOI:10.1107/S0365110X65000439.

Povezano

[1] Merck Index, 11th Edition, 6315.

[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

[6] Gaultier, J.; Hauw, C. (1965). „Structure de l'α-Naphtoquinone”. Acta Crystallographica 18 (2): 179–183. DOI:10.1107/S0365110X65000439.

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