3,4′-Dihydroxystilbene

3,4′-Dihydroxystilbene
Chemical strucrure of 3,4'-dihydroxystilbene
Names
IUPAC name
3-[2-(4-hydroxyphenyl)ethenyl]phenol
Identifiers
CAS Number
  • 63877-76-9 checkY
  • 62574-04-3 (non-specific) checkY
3D model (JSmol)
  • (trans): Interactive image
ChemSpider
  • 8346853 (trans)
PubChem CID
  • 54350316
  • 10171348 (trans)
UNII
  • 4DC9L42B37 checkY
CompTox Dashboard (EPA)
  • DTXSID00710753 Edit this at Wikidata
InChI
  • InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H/b5-4+
    Key: UFGKEFGYNRJIGO-SNAWJCMRSA-N
  • InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H
    Key: UFGKEFGYNRJIGO-UHFFFAOYSA-N
  • (trans): InChI=1/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H/b5-4+
    Key: UFGKEFGYNRJIGO-SNAWJCMRBG
  • (trans): Oc2cc(/C=C/c1ccc(O)cc1)ccc2
Properties
Chemical formula
 C14H12O2
Molar mass 212.24 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

3,4′-Dihydroxystilbene is a stilbenoid found in the roots of Hydrangea macrophylla.[1]

See also

  • 4,4'-Dihydroxystilbene
  • Resveratrol

References

  1. ^ Lunularic acid and related compounds in liverworts, algae and Hydrangea. John Gorham, Phytochemistry, 1977, Volume 16, Issue 2, Pages 249–253, doi:10.1016/S0031-9422(00)86795-3


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Hydroxystilbenes and their glycosides (monomeric forms)
Dihydroxylated
  • Pinosylvin
  • 3,4′-Dihydroxystilbene
Trihydroxylated
  • Resveratrol
TetrahydroxylatedO-methylated
Combretastatins
carboxylatedother acylationsGlycosides
of resveratrol
of rhapontigenin
  • Rhapontigenin 3-O-rutinoside
    • 4'-Methoxy-(E)-resveratrol 3-O-rutinoside
  • Rhaponticin (Rhapontigenin glucoside)
Oligomeric forms


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