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3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

group of stereoisomers with the chemical formula C₂₀H₂₂O₆
ChemicalSubstance group_of_stereoisomers Q105160505
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3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

Summary

3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one is a group of stereoisomers[1].

Key Facts

  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's instance of is recorded as group of stereoisomers[2].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's canonical SMILES is recorded as O=C1OCC(CC2=CC=C(O)C(OC)=C2)C1CC3=CC=C(O)C(OC)=C3[3].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's InChI is recorded as InChI=1S/C20H22O6/c1-24-18-9-12(3-5-16(18)21)7-14-11-26-20(23)15(14)8-13-4-6-17(22)19(10-13)25-2/h3-6,9-10,14-15,21-22H,7-8,11H2,1-2H3[4].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's InChIKey is recorded as MATGKVZWFZHCLI-UHFFFAOYSA-N[5].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's chemical formula is recorded as C₂₀H₂₂O₆[6].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's subclass of is recorded as chemical compound[7].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's PubChem CID is recorded as 345761[8].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Pinus sylvestris[9].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Trachelospermum lucidum[10].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Forsythia viridissima[11].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Artemisia porrecta[12].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Forsythia suspensa[13].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Diospyros japonica[14].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Diospyros glaucifolia[15].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Daphne odora[16].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Artemisia giraldii[17].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Daphne genkwa[18].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Selaginella[19].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Daphne oleoides[20].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Forsythia ovata[21].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Piper philippinum[22].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's found in taxon is recorded as Piper kwashoense[23].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+358.141638424'}[24].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's SureChEMBL ID is recorded as 13505961[25].
  • 3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one's SureChEMBL ID is recorded as 29617982[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Phenolic extractives from the bark of Pinus sylvestris L. and their effects on inflammatory mediators nitric oxide and prostaglandin E2.. wikidata.org.
  9. [10] ↑ . Isolation of a New Lipoxygenase Active Saponin and a New Triterpenoid from the Leaves of Trachelospermum lucidum. wikidata.org.
  10. [11] ↑ . (+)-Pinoresinol/(+)-lariciresinol reductase from Forsythia intermedia. Protein purification, cDNA cloning, heterologous expression and comparison to isoflavone reductase. wikidata.org.
  11. [12] ↑ . Cytotoxic terpenoids and flavonoids from Artemisia annua. wikidata.org.
  12. [13] ↑ . (+)-Pinoresinol/(+)-lariciresinol reductase from Forsythia intermedia. Protein purification, cDNA cloning, heterologous expression and comparison to isoflavone reductase. wikidata.org.
  13. [14] ↑ . Antibacterial activity of diosquinone isolated from Diospyros tricolor. wikidata.org.
  14. [15] ↑ . Antibacterial activity of diosquinone isolated from Diospyros tricolor. wikidata.org.
  15. [16] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  16. [17] ↑ . Cytotoxic terpenoids and flavonoids from Artemisia annua. wikidata.org.
  17. [18] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  18. [19] ↑ . Phenolic Constituents of Selaginella doederleinii. wikidata.org.
  19. [20] ↑ . Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. wikidata.org.
  20. [21] ↑ . Novel benzylic ether reductions in lignan biogenesis in Forsythia intermedia. wikidata.org.
  21. [22] ↑ . Constituents from Piper divaricatum. wikidata.org.
  22. [23] ↑ . Lignans, an amide and anti-platelet activities from Piper philippinum. wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_3-4-bis-4-hydroxy-3-methoxyphenyl-methyl-oxolan-2-one_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one}}, year = {2026}, url = {https://4ort.xyz/entity/3-4-bis-4-hydroxy-3-methoxyphenyl-methyl-oxolan-2-one}, note = {Accessed: 2026-05-03}}
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