3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one

pair of enantiomers
ChemicalSubstance group_of_stereoisomers Q105205211
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3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one

Summary

3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one is a group of stereoisomers[1].

Key Facts

  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's instance of is recorded as group of stereoisomers[2].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's chemical structure is recorded as Phyllodulcin racemic.svg[3].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's CAS Registry Number is recorded as 55555-33-4[4].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's canonical SMILES is recorded as O=C1OC(C2=CC=C(OC)C(O)=C2)CC=3C=CC=C(O)C13[5].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's InChI is recorded as InChI=1S/C16H14O5/c1-20-13-6-5-9(7-12(13)18)14-8-10-3-2-4-11(17)15(10)16(19)21-14/h2-7,14,17-18H,8H2,1H3[6].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's InChIKey is recorded as PBILBHLAPJTJOT-UHFFFAOYSA-N[7].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's chemical formula is recorded as C₁₆H₁₄O₅[8].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's subclass of is recorded as chemical compound[9].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's PubChem CID is recorded as 164615[10].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's ChEBI ID is recorded as 174724[11].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's found in taxon is recorded as Hydrangea macrophylla[12].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's Human Metabolome Database ID is recorded as HMDB0030807[13].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+286.084123548'}[14].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's SureChEMBL ID is recorded as 12205058[15].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's SureChEMBL ID is recorded as 30460064[16].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's DSSTox substance ID is recorded as DTXSID101029761[17].
  • 3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one's UniChem compound ID is recorded as 32014006[18].

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] . SciFinder. wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . ChEBI release 2022-06-13. wikidata.org.
  11. [12] . New type of anti-diabetic compounds from the processed leaves of Hydrangea macrophylla var. thunbergii (Hydrangeae Dulcis Folium).. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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MLA “3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-4-dihydro-8-hydroxy-3-3-hydroxy-4-methoxyphenyl-1h-2-benzopyran-1-one.
BibTeX @misc{4ortxyz_3-4-dihydro-8-hydroxy-3-3-hydroxy-4-methoxyphenyl-1h-2-benzopyran-1-one_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl) 1H-2-benzopyran-1-one}}, year = {2026}, url = {https://4ort.xyz/entity/3-4-dihydro-8-hydroxy-3-3-hydroxy-4-methoxyphenyl-1h-2-benzopyran-1-one}, note = {Accessed: 2026-05-03}}
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