p-coumaryl alcohol

chemical compound
ChemicalSubstance type_of_chemical_entity Q420084
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p-coumaryl alcohol

Summary

p-coumaryl alcohol is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • p-coumaryl alcohol's instance of is recorded as type of chemical entity[3].
  • p-coumaryl alcohol's chemical structure is recorded as P-Coumaryl alcohol.svg[4].
  • p-coumaryl alcohol's CAS Registry Number is recorded as 20649-40-5[5].
  • p-coumaryl alcohol's canonical SMILES is recorded as C1=CC(=CC=C1C=CCO)O[6].
  • p-coumaryl alcohol's InChI is recorded as InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+[7].
  • p-coumaryl alcohol's InChIKey is recorded as PTNLHDGQWUGONS-OWOJBTEDSA-N[8].
  • p-coumaryl alcohol's chemical formula is recorded as C₉H₁₀O₂[9].
  • p-coumaryl alcohol's subclass of is recorded as 4-hydroxycinnamyl alcohol[10].
  • p-coumaryl alcohol's Commons category is recorded as Paracoumaryl alcohol[11].
  • p-coumaryl alcohol's ChEMBL ID is recorded as CHEMBL109034[12].
  • p-coumaryl alcohol's Freebase ID is recorded as /m/0f9n4k[13].
  • p-coumaryl alcohol's UNII is recorded as 61POZ1QQ11[14].
  • p-coumaryl alcohol's ChemSpider ID is recorded as 4444166[15].
  • p-coumaryl alcohol's PubChem CID is recorded as 5280535[16].
  • p-coumaryl alcohol's KEGG ID is recorded as C02646[17].
  • p-coumaryl alcohol's ChEBI ID is recorded as 64555[18].
  • p-coumaryl alcohol's found in taxon is recorded as Alpinia galanga[19].
  • p-coumaryl alcohol's found in taxon is recorded as Cardiocrinum cordatum[20].
  • p-coumaryl alcohol's found in taxon is recorded as Alpinia officinarum[21].
  • p-coumaryl alcohol's found in taxon is recorded as Rhodiola rosea[22].
  • p-coumaryl alcohol's found in taxon is recorded as Daucus carota[23].
  • p-coumaryl alcohol's found in taxon is recorded as potato[24].
  • p-coumaryl alcohol's Reaxys registry number is recorded as 2961090[25].
  • p-coumaryl alcohol's isomeric SMILES is recorded as C1=CC(=CC=C1/C=C/CO)O[26].
  • p-coumaryl alcohol's Human Metabolome Database ID is recorded as HMDB0003654[27].

Why It Matters

p-coumaryl alcohol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] It is known by 18 alternative names across languages and contexts.[29]

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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI. Retrieved . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . Antiallergic principles from Alpinia galanga: structural requirements of phenylpropanoids for inhibition of degranulation and release of TNF-alpha and IL-4 in RBL-2H3 cells. wikidata.org.
  18. [20] . Flavonol and phenylpropanoid glycosides from Lilium cordatum. wikidata.org.
  19. [21] . Isolation and characterization of some antioxidative compounds from the rhizomes of smaller galanga (Alpinia officinarum Hance).. wikidata.org.
  20. [22] . Phenylpropanoids of a callus culture of Rhodiola rosea. wikidata.org.
  21. [23] . Biosynthesis of methyleugenol and methylisoeugenol in Daucus carota leaves: Characterization of eugenol/isoeugenol synthase and O-Methyltransferase. wikidata.org.
  22. [24] . Biochemical characterization of the suberization-associated anionic peroxidase of potato. wikidata.org.
  23. [25] . ChEBI. Retrieved . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). p-coumaryl alcohol. Retrieved May 3, 2026, from https://4ort.xyz/entity/p-coumaryl-alcohol
MLA “p-coumaryl alcohol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/p-coumaryl-alcohol.
BibTeX @misc{4ortxyz_p-coumaryl-alcohol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{p-coumaryl alcohol}}, year = {2026}, url = {https://4ort.xyz/entity/p-coumaryl-alcohol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): p-coumaryl alcohol — https://4ort.xyz/entity/p-coumaryl-alcohol (retrieved 2026-05-03)

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