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Veratrole alcohol
Names

Preferred IUPAC name (3,4-Dimethoxyphenyl)methanol
Other names Veratryl alcohol 3,4-Dimethoxybenzyl alcohol
Identifiers
CAS Number	93-03-8^Y
3D model (JSmol)	Interactive image
ChemSpider	6851^N
ECHA InfoCard	100.002.012
PubChem CID	7118
UNII	MB4T4A711H^Y
CompTox Dashboard (EPA)
InChI InChI=1S/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3^N Key: OEGPRYNGFWGMMV-UHFFFAOYSA-N^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). N verify (what is ^YN ?) 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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This page was last edited on 24 January 2023, at 06:11