Veratrole alcohol

Veratrole alcohol
Names
	IUPAC name (3,4-Dimethoxyphenyl)methanol
	Other names Veratryl alcohol; 3,4-Dimethoxybenzylalcohol
Identifiers
CAS Number	93-03-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	6851 ;
ECHA InfoCard	100.002.012
PubChem CID	7118;
UNII	MB4T4A711H ;
CompTox Dashboard (EPA)	DTXSID1059076 ;
	InChI InChI=1S/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3 Key: OEGPRYNGFWGMMV-UHFFFAOYSA-N ; InChI=1/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3 Key: OEGPRYNGFWGMMV-UHFFFAOYAK;
	SMILES O(c1ccc(cc1OC)CO)C;
Properties
Chemical formula	C9H12O3
Molar mass	168.192 g·mol−1
Boiling point	296 to 297 °C (565 to 567 °F; 569 to 570 K) 732 Torr[1]
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Veratrole alcohol (veratryl alcohol) is an organic compound related to veratrole and also to benzyl alcohol. It can be obtained by reduction of veratraldehyde.[2] Veratrole alcohol is the raw material for the synthesis of cyclotriveratrylene which is used in host–guest chemistry. It is a secondary metabolite of some white rot fungi and is believed to play a role in their degradation of lignin.[3]

References

CRC Handbook of Tables for Organic Compound Identification, Third Edition, 1984, ISBN 0-8493-0303-6.
Hermann Kämmerer, V.; Casacuberta, A. O. (1963). "Zur darstellung von phenolalkoholen aus phenolaldehyden mit wasserstoff/RANEY-nickel und aus phenolcarbonsäureestern mit LiAlH4". Die Makromolekulare Chemie. 67: 167–172. doi:10.1002/macp.1963.020670116.
Zapanta, L. S.; Tien, M. (1997). "The roles of veratryl alcohol and oxalate in fungal lignin degradation". Journal of Biotechnology. 53 (2–3): 93–102. doi:10.1016/S0168-1656(96)01678-1.

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