1-Naftol

1-Naftol
	Naphthalen-1-ol
Drugi nazivi	1-Hidroksinaftalen; 1-Naftalenol; alfa-Naftol
Identifikacija
CAS registarski broj	90-15-3
PubChem	7005
ChemSpider	6739
UNII	2A71EAQ389
KEGG	C11714
ChEBI	10319
ChEMBL	CHEMBL122617
Jmol-3D slike	Slika 1
SMILES
	Oc2cccc1ccccc12
InChI
	InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H ; Kod: KJCVRFUGPWSIIH-UHFFFAOYSA-N InChI=1/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H; Kod: KJCVRFUGPWSIIH-UHFFFAOYAZ
Svojstva
Molekulska formula	C10H8O
Molarna masa	144.17 g/mol
Agregatno stanje	bezbojna ili bela čvrsta materija
Gustina	1.10 g/cm3
Tačka topljenja	95-96 °C
Tačka ključanja	278–280 °C
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1-Naftol, ili α-naftol, je bezbojna kristalna materija sa formulom C₁₀H₇OH.^[6] On je izomer 2-naftola od koga se razlikuje po lokaciji hidroksilne grupe na naftalenu. Naftoli su naftalenski homolozi fenola. Njihova hidroksilna grupa je reaktivnija od fenolne. Oba izomera su rastvorana u jednostavnim alkoholima, etrima, i hloroformu. Oni mogu da se koriste u proizvodnji boja i organskoj sintezi.

1-Naftol je metabolit insekticida karbarila i naftalena. Kao i za TCPy, za njega je pokazano da snižava nivoe testosterona kod ljudi.^[7]

Literatura

↑ 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
↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
↑ 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 21948863. edit
↑ Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
↑ Meeker, John D.; Ryan, Louise; Barr, Dana B.; Hauser, Russ (January 2006). „Exposure to Nonpersistent Insecticides and Male Reproductive Hormones”. Epidemiology 17 (1): 61–68. DOI:10.1097/01.ede.0000190602.14691.70. PMID 16357596.

Spoljašnje veze

Portal Hemija

NIST hemijska veb-knjiga 1-naftalenol

[1] 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

[2] 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.

[3] 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

[4] Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[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 21948863. edit

[Clayden1st-6] Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.

[7] Meeker, John D.; Ryan, Louise; Barr, Dana B.; Hauser, Russ (January 2006). „Exposure to Nonpersistent Insecticides and Male Reproductive Hormones”. Epidemiology 17 (1): 61–68. DOI:10.1097/01.ede.0000190602.14691.70. PMID 16357596.

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