9-Anthracenemethanol

9-Anthracenemethanol
Names
	Preferred IUPAC name (Anthracen-9-yl)methanol
Identifiers
CAS Number	1468-95-7;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3188668;
ChemSpider	66482;
ECHA InfoCard	100.014.544
EC Number	215-998-5;
PubChem CID	73848;
CompTox Dashboard (EPA)	DTXSID1049221 ;
	InChI InChI=1S/C15H12O/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9,16H,10H2 Key: JCJNNHDZTLRSGN-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C=C3C=CC=CC3=C2CO;
Properties
Chemical formula	C15H12O
Molar mass	208.260 g·mol−1
Appearance	white solid
Melting point	158 °C (316 °F; 431 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H341
Precautionary statements	P201, P202, P281, P308+P313, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

9-Anthracenemethanol is the derivative of anthracene with a hydroxymethyl group (CH₂OH) attached to the 9-position. It is a colorless solid that is soluble in ordinary organic solvents. The compound can be prepared by hydrogenation of 9-anthracenecarboxaldehyde. It is a versatile precursor to supramolecular assemblies.^[1]

References[]

^ Goshe, A. J.; Steele, I. M.; Ceccarelli, C.; Rheingold, A. L.; Bosnich, B. (2002). "Supramolecular recognition: On the kinetic lability of thermodynamically stable host-guest association complexes". Proceedings of the National Academy of Sciences. 99 (8): 4823–4829. doi:10.1073/pnas.052587499. PMC 122677. PMID 11959933.

[1] Goshe, A. J.; Steele, I. M.; Ceccarelli, C.; Rheingold, A. L.; Bosnich, B. (2002). "Supramolecular recognition: On the kinetic lability of thermodynamically stable host-guest association complexes". Proceedings of the National Academy of Sciences. 99 (8): 4823–4829. doi:10.1073/pnas.052587499. PMC 122677. PMID 11959933.

[1]