4-hydroxycoumarin

chemical compound
ChemicalSubstance type_of_chemical_entity Q25323691
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4-hydroxycoumarin

Summary

4-hydroxycoumarin is a type of chemical entity[1]. 4-hydroxycoumarin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2]

Key Facts

  • 4-hydroxycoumarin's instance of is recorded as type of chemical entity[3].
  • 4-hydroxycoumarin's chemical structure is recorded as 4-Hydroxycoumarin.PNG[4].
  • 4-hydroxycoumarin's CAS Registry Number is recorded as 1076-38-6[5].
  • 4-hydroxycoumarin's EC number is recorded as 214-060-2[6].
  • 4-hydroxycoumarin's canonical SMILES is recorded as C1=CC=C2C(=C1)C(=CC(=O)O2)O[7].
  • 4-hydroxycoumarin's InChI is recorded as InChI=1S/C9H6O3/c10-7-5-9(11)12-8-4-2-1-3-6(7)8/h1-5,10H[8].
  • 4-hydroxycoumarin's InChIKey is recorded as VXIXUWQIVKSKSA-UHFFFAOYSA-N[9].
  • 4-hydroxycoumarin's chemical formula is recorded as C₉H₆O₃[10].
  • 4-hydroxycoumarin's subclass of is recorded as biogenic coumarin[11].
  • 4-hydroxycoumarin's part of is recorded as 4-hydroxycoumarin metabolic process[12].
  • 4-hydroxycoumarin's part of is recorded as 4-hydroxycoumarin catabolic process[13].
  • 4-hydroxycoumarin's part of is recorded as 4-hydroxycoumarin biosynthetic process[14].
  • 4-hydroxycoumarin's Commons category is recorded as 4-Hydroxycoumarin[15].
  • 4-hydroxycoumarin's ChEMBL ID is recorded as CHEMBL301141[16].
  • 4-hydroxycoumarin's PDB structure ID is recorded as 1V5Y[17].
  • 4-hydroxycoumarin's UNII is recorded as X954ZLL2RD[18].
  • 4-hydroxycoumarin's ChemSpider ID is recorded as 10254753[19].
  • 4-hydroxycoumarin's PubChem CID is recorded as 54682930[20].
  • 4-hydroxycoumarin's ChEBI ID is recorded as 40070[21].
  • 4-hydroxycoumarin's found in taxon is recorded as Cullen drupaceum[22].
  • 4-hydroxycoumarin's found in taxon is recorded as Vitis vinifera[23].
  • 4-hydroxycoumarin's found in taxon is recorded as Ruta graveolens[24].
  • 4-hydroxycoumarin's DrugBank ID is recorded as DB03410[25].
  • 4-hydroxycoumarin's Reaxys registry number is recorded as 129768[26].
  • 4-hydroxycoumarin's mass is recorded as {'unit': 'Q483261', 'amount': '+162.032'}[27].

Why It Matters

4-hydroxycoumarin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (17 views/month).[2] 4-hydroxycoumarin is known by 9 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ChEMBL. Retrieved . wikidata.org.
  15. [17] . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] . Global Substance Registration System. Retrieved . wikidata.org.
  17. [19] . Q2311683. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . ChEBI. Retrieved . wikidata.org.
  20. [22] . Phenolic components of the unsaponifiable fraction of the lipids of Psorlea drupaceae. wikidata.org.
  21. [23] . RP-HPLC analysis of phenolic compounds and flavonoids in beverages and plant extracts using a CoulArray detector.. wikidata.org.
  22. [24] . Potential allelochemicals fromRuta graveolens L. and their action on radish seeds. wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . ChEBI. Retrieved . wikidata.org.
  25. [27] . PubChem. Retrieved . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). 4-hydroxycoumarin. Retrieved May 3, 2026, from https://4ort.xyz/entity/4-hydroxycoumarin
MLA “4-hydroxycoumarin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/4-hydroxycoumarin.
BibTeX @misc{4ortxyz_4-hydroxycoumarin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{4-hydroxycoumarin}}, year = {2026}, url = {https://4ort.xyz/entity/4-hydroxycoumarin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 4-hydroxycoumarin — https://4ort.xyz/entity/4-hydroxycoumarin (retrieved 2026-05-03)

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