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levomenol

chemical compound
ChemicalSubstance type_of_chemical_entity Q179896
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levomenol

Summary

levomenol is a type of chemical entity[1]. levomenol ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (79 views/month).[2]

Key Facts

  • levomenol's instance of is recorded as type of chemical entity[3].
  • levomenol's chemical structure is recorded as Bisabolol alpha minus.svg[4].
  • levomenol's CAS Registry Number is recorded as 23089-26-1[5].
  • levomenol's EC number is recorded as 245-423-3[6].
  • levomenol's canonical SMILES is recorded as CC1=CCC(CC1)C(C)(CCC=C(C)C)O[7].
  • levomenol's InChI is recorded as InChI=1S/C15H26O/c1-12(2)6-5-11-15(4,16)14-9-7-13(3)8-10-14/h6-7,14,16H,5,8-11H2,1-4H3/t14-,15+/m1/s1[8].
  • levomenol's InChIKey is recorded as RGZSQWQPBWRIAQ-CABCVRRESA-N[9].
  • levomenol's chemical formula is recorded as C₁₅H₂₆O[10].
  • levomenol's subclass of is recorded as (2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol[11].
  • levomenol's Commons category is recorded as Bisabolol[12].
  • levomenol's has part is recorded as carbon[13].
  • levomenol's has part is recorded as hydrogen[14].
  • levomenol's has part is recorded as oxygen[15].
  • levomenol's ChEMBL ID is recorded as CHEMBL1096927[16].
  • levomenol's Freebase ID is recorded as /m/097nbn[17].
  • levomenol's UNII is recorded as 24WE03BX2T[18].
  • levomenol's ChemSpider ID is recorded as 390796[19].
  • levomenol's PubChem CID is recorded as 442343[20].
  • levomenol's KEGG ID is recorded as C09621[21].
  • levomenol's ChEBI ID is recorded as 125[22].
  • levomenol's found in taxon is recorded as Matricaria chamomilla[23].
  • levomenol's found in taxon is recorded as Eremanthus arboreus[24].
  • levomenol's found in taxon is recorded as Ferula hermonis[25].
  • levomenol's found in taxon is recorded as Santolina canescens[26].
  • levomenol's found in taxon is recorded as Achillea odorata[27].

Why It Matters

levomenol ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (79 views/month).[2] levomenol has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[28] levomenol is known by 9 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] ↑ . 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] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . ChEMBL. Retrieved . wikidata.org.
  15. [17] ↑ . Freebase Data Dumps. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  21. [23] ↑ . Volatile secondary metabolite pattern of callus cultures of Chamomilla recutita.. wikidata.org.
  22. [24] ↑ . Volatile Constituents of Leaves, Bark and Wood FromVanillosmopsis arboreaBaker.. wikidata.org.
  23. [25] ↑ . Daucane sesquiterpenes from Ferula hermonis. wikidata.org.
  24. [26] ↑ . Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring. wikidata.org.
  25. [27] ↑ . Bisabolene derivatives and other constituents fromAchillea odorata. 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). levomenol. Retrieved May 3, 2026, from https://4ort.xyz/entity/levomenol
MLA “levomenol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/levomenol.
BibTeX @misc{4ortxyz_levomenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{levomenol}}, year = {2026}, url = {https://4ort.xyz/entity/levomenol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): levomenol — https://4ort.xyz/entity/levomenol (retrieved 2026-05-03)

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