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totarol

chemical compound
ChemicalSubstance type_of_chemical_entity Q7828277
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totarol

Summary

totarol is a type of chemical entity[1]. totarol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 views/month).[2]

Key Facts

  • totarol's instance of is recorded as type of chemical entity[3].
  • totarol's chemical structure is recorded as Totarol.svg[4].
  • totarol's CAS Registry Number is recorded as 511-15-9[5].
  • totarol's EC number is recorded as 622-932-2[6].
  • totarol's canonical SMILES is recorded as CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O[7].
  • totarol's InChI is recorded as InChI=1S/C20H30O/c1-13(2)18-14-7-10-17-19(3,4)11-6-12-20(17,5)15(14)8-9-16(18)21/h8-9,13,17,21H,6-7,10-12H2,1-5H3/t17-,20+/m0/s1[8].
  • totarol's InChIKey is recorded as ZRVDANDJSTYELM-FXAWDEMLSA-N[9].
  • totarol's chemical formula is recorded as C₂₀H₃₀O[10].
  • totarol's subclass of is recorded as (4bS)-1-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol[11].
  • totarol's Commons category is recorded as Totarol[12].
  • totarol's ChEMBL ID is recorded as CHEMBL487602[13].
  • totarol's Freebase ID is recorded as /m/09k610x[14].
  • totarol's UNII is recorded as 67NH2854WW[15].
  • totarol's ChemSpider ID is recorded as 83757[16].
  • totarol's PubChem CID is recorded as 92783[17].
  • totarol's ChEBI ID is recorded as 69241[18].
  • totarol's found in taxon is recorded as Thuja occidentalis[19].
  • totarol's found in taxon is recorded as Thujopsis dolabrata[20].
  • totarol's found in taxon is recorded as Chamaecyparis obtusa[21].
  • totarol's found in taxon is recorded as Chamaecyparis pisifera[22].
  • totarol's found in taxon is recorded as Juniperus communis[23].
  • totarol's found in taxon is recorded as Chamaecyparis formosensis[24].
  • totarol's found in taxon is recorded as Tetraclinis articulata[25].
  • totarol's found in taxon is recorded as Apis mellifera[26].
  • totarol's found in taxon is recorded as Juniperus phoenicea[27].

Why It Matters

totarol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 views/month).[2]

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] ↑ . ECHA Substance Infocard database. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . ChEMBL. Retrieved . wikidata.org.
  17. [19] ↑ . Contribution to the Study of the Essential Oil of Thuja occidentalis L.. wikidata.org.
  18. [20] ↑ . Diterpene production by callus of some plants belonging to cupressaceae.. wikidata.org.
  19. [21] ↑ . Diterpene production by callus of some plants belonging to cupressaceae.. wikidata.org.
  20. [22] ↑ . Diterpene production by callus of some plants belonging to cupressaceae.. wikidata.org.
  21. [23] ↑ . Antimycobacterial terpenoids from Juniperus communis L. (Cuppressaceae).. wikidata.org.
  22. [24] ↑ . Terpenes and lignans from leaves of Chamaecyparis formosensis. wikidata.org.
  23. [25] ↑ . Diterpenoids from Tetraclinis articulata that inhibit various human leukocyte functions. wikidata.org.
  24. [26] ↑ . Characterization and antioxidant properties of six Algerian propolis extracts: ethyl acetate extracts inhibit myeloperoxidase activity. wikidata.org.
  25. [27] ↑ . Chemical compounds from Phoenician juniper berries (Juniperus phoenicea). wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). totarol. Retrieved May 3, 2026, from https://4ort.xyz/entity/totarol
MLA “totarol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/totarol.
BibTeX @misc{4ortxyz_totarol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{totarol}}, year = {2026}, url = {https://4ort.xyz/entity/totarol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): totarol — https://4ort.xyz/entity/totarol (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20w ago · Shuaib-bot bot · 2026-05-02 view diff on Wikidata ↗
    Instance of → —
    Stereoisomer of → cis-totarol
    Found in taxon → Thuja occidentalis, Thujopsis dolabrata, Chamaecyparis obtusa +27
    Subclass of → (4bS)-1-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.