2-Hlorofenol

2-Hlorophenol
2-Chlorophenol	2-Chlorophenol
	2-Hlorofenol
Drugi nazivi	2-Hidroksihlorobenzen, o-Hlorofenol
Identifikacija
CAS registarski broj	95-57-8
ChemSpider	13837686
DrugBank	DB03110
KEGG	C14219
ChEBI	47083
ChEMBL	CHEMBL108877
Jmol-3D slike	Slika 1
SMILES
	Oc1ccccc1Cl
InChI
	InChI=1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H ; Kod: ISPYQTSUDJAMAB-UHFFFAOYSA-N InChI=1/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H; Kod: ISPYQTSUDJAMAB-UHFFFAOYAM
Svojstva
Molekulska formula	C6H5ClO
Molarna masa	128,56 g/mol
Agregatno stanje	Svetli ćilibar, tečnost
Gustina	1,2634 g/cm3 na 20 °C
Tačka topljenja	9.4 °C
Tačka ključanja	174.9 °C
Rastvorljivost u vodi	20 g/L na 20 °C
Rastvorljivost	rastvoran u etanolu, dietil etru, benzenu
Napon pare	0,308 kPa
pKa	8,56
Termohemija
Specifični toplotni kapacitet, C	1,468 J·g-1·K-1
Opasnost
Podaci o bezbednosti prilikom rukovanja (MSDS)	MSDS
Opasnost u toku rada	Korozivan - uzrokuje opekotine
Tačka paljenja	64 °C
Tačka spontanog paljenja	550 °C
Srodna jedinjenja
Srodna aromatični; ugljovodonici	benzen; fenol; hlorobenzen
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

2-Areni ili orto-hlorofenol je organsko jedinjenje, derivat fenola. Srodna jedinjenja se koriste kao dezinfektivni agensi i pesticidi. Ovo jedinjenje ima mali broj primena, ali je intermedijer u polihlorinaciji fhenola.^[8]

Povezano

Hlorofenol

Reference

↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 3–120, ISBN 0-8493-0863-2
↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 1281, ISBN 0-8493-0863-2
↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 8–103, ISBN 0-8493-0863-2
↑ Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 15–18, ISBN 0-8493-0863-2
↑ 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
↑ Fiege, H.; Voges, H.-M.; Hamamoto, T; Umemura, S.; Iwata, T.; Miki, H.; Fujita, Y.; Buysch, H.-J.; Garbe, D.; Paulus, W. (2000), „Phenol Derivatives”, Ullmann's Encyclopedia of Industrial Chemistry (Weinheim: Wiley-VCH), DOI:10.1002/14356007.a19_313

Spoljašnje veze

Portal Hemija

ToxFAQs for Chlorophenols, Agency for Toxic Substances and Disease Registry.

[hand-1] Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 3–120, ISBN 0-8493-0863-2

[hand2-2] Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 1281, ISBN 0-8493-0863-2

[hand3-3] Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 8–103, ISBN 0-8493-0863-2

[hand4-4] Lide, David R. (1998), Handbook of Chemistry and Physics (87 izd.), Boca Raton, FL: CRC Press, pp. 15–18, ISBN 0-8493-0863-2

[5] 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

[6] 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.

[7] 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

[8] Fiege, H.; Voges, H.-M.; Hamamoto, T; Umemura, S.; Iwata, T.; Miki, H.; Fujita, Y.; Buysch, H.-J.; Garbe, D.; Paulus, W. (2000), „Phenol Derivatives”, Ullmann's Encyclopedia of Industrial Chemistry (Weinheim: Wiley-VCH), DOI:10.1002/14356007.a19_313

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