2-Hydroxy-4-methoxybenzaldehyde

2-Hydroxy-4-methoxybenzaldehyde
Chemical structure of 2-hydroxy-4-methoxybenzaldehyde
Names
Preferred IUPAC name
2-Hydroxy-4-methoxybenzaldehyde
Other names
4-Methoxysalicylaldehyde
Identifiers
CAS Number
  • 673-22-3 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 62803
ECHA InfoCard 100.010.550 Edit this at Wikidata
PubChem CID
  • 69600
UNII
  • 2N395P88LW checkY
CompTox Dashboard (EPA)
  • DTXSID1060970 Edit this at Wikidata
InChI
  • InChI=1S/C8H8O3/c1-11-7-3-2-6(5-9)8(10)4-7/h2-5,10H,1H3
    Key: WZUODJNEIXSNEU-UHFFFAOYSA-N
  • COC1=CC(=C(C=C1)C=O)O
Properties
Chemical formula
 C8H8O3
Molar mass 152.149 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

2-Hydroxy-4-methoxybenzaldehyde is a chemical compound and an isomer of vanillin. Urolithin M7, one of the urolithins, has also been synthesized from 2-hydroxy-4-methoxybenzaldehyde using the inverse electron-demand Diels–Alder reaction.[1]

See also

  • Vanillin
  • 2-Hydroxy-5-methoxybenzaldehyde
  • Isovanillin
  • ortho-Vanillin

References

  1. ^ Bodwell, Graham; Pottie, Ian; Nandaluru, Penchal (2011). "An Inverse Electron-Demand Diels-Alder-Based Total Synthesis of Urolithin M7". Synlett. 2011 (15): 2245. doi:10.1055/s-0030-1261203.


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