Fluorenol information

Fluorenol^[1]
Names
	IUPAC name 9H-Fluoren-9-ol
	Other names 9-Hydroxyfluorene
Identifiers
CAS Number	1689-64-1 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:16904 ;
ChemSpider	66916 ;
ECHA InfoCard	100.015.345
EC Number	216-879-0;
PubChem CID	74318;
UNII	BV0Q72R613 ;
CompTox Dashboard (EPA)	DTXSID4052683 ;
	InChI InChI=1S/C13H10O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13-14H Key: AFMVESZOYKHDBJ-UHFFFAOYSA-N ; InChI=1/C13H10O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13-14H Key: AFMVESZOYKHDBJ-UHFFFAOYAM;
	SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)O;
Properties
Chemical formula	C13H10O
Molar mass	182.22 g/mol
Appearance	Off-white crystalline powder
Density	1.151 g/mL
Melting point	152 to 155 °C (306 to 311 °F; 425 to 428 K)
Solubility in water	Practically insoluble
Hazards
NFPA 704 (fire diamond)	0 0 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Fluorenol, also known as hydrafinil,^[3] is an alcohol derivative of fluorene. In the most significant isomer, fluoren-9-ol or 9-hydroxyfluorene, the hydroxy group is located on the bridging carbon between the two benzene rings. Hydroxyfluorene can be converted to fluorenone by oxidation. It is a white-cream colored solid at room temperature.

^ 9-Hydroxyfluorene, chemicalland21.com
^ Record of 9H-Fluoren-9-ol in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 5 November 2008.
^ Knoop, Andre; Fußhöller, Gregor; Haenelt, Nadine; Goergens, Christian; Guddat, Sven; Geyer, Hans; Thevis, Mario (November 2021). "Mass spectrometric characterization of urinary hydrafinil metabolites for routine doping control purposes". Drug Testing and Analysis. 13 (11–12): 1915–1920. doi:10.1002/dta.3137. ISSN 1942-7611. PMID 34378339. S2CID 236976954.

[1] 9-Hydroxyfluorene, chemicalland21.com

[GESTIS-2] Record of 9H-Fluoren-9-ol in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 5 November 2008.

[3] Knoop, Andre; Fußhöller, Gregor; Haenelt, Nadine; Goergens, Christian; Guddat, Sven; Geyer, Hans; Thevis, Mario (November 2021). "Mass spectrometric characterization of urinary hydrafinil metabolites for routine doping control purposes". Drug Testing and Analysis. 13 (11–12): 1915–1920. doi:10.1002/dta.3137. ISSN 1942-7611. PMID 34378339. S2CID 236976954.

Fluorenol information

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