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Veratrole alcohol






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From Wikipedia, the free encyclopedia
 


Veratrole alcohol
Veratrole alcohol
Names
Preferred IUPAC name

(3,4-Dimethoxyphenyl)methanol

Other names

Veratryl alcohol
3,4-Dimethoxybenzyl alcohol

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.002.012 Edit this at Wikidata

PubChem CID

UNII

CompTox Dashboard (EPA)

  • 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

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 checkY☒N ?)

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[edit]

  1. ^ 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.

  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Veratrole_alcohol&oldid=1135365035"

    Categories: 
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    This page was last edited on 24 January 2023, at 06:11 (UTC).

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