Veratrole alcohol

Veratrole alcohol
Names
Preferred IUPAC name
(3,4-Dimethoxyphenyl)methanol
Other names
Veratryl alcohol
3,4-Dimethoxybenzyl alcohol
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.012
UNII
  • 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
  • O(c1ccc(cc1OC)CO)C
Properties
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

  1. ^ CRC Handbook of Tables for Organic Compound Identification, Third Edition, 1984, ISBN 0-8493-0303-6.
  2. ^ 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.
  3. ^ 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.