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oct-1-en-3-ol

chemical compound
ChemicalSubstance group_of_stereoisomers Q161667
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oct-1-en-3-ol

Summary

oct-1-en-3-ol is a group of stereoisomers[1]. oct-1-en-3-ol draws 27 Wikipedia views per month (group_of_stereoisomers category, ranking #191 of 1,063).[2]

Key Facts

  • oct-1-en-3-ol's instance of is recorded as group of stereoisomers[3].
  • oct-1-en-3-ol's chemical structure is recorded as Octenol.png[4].
  • oct-1-en-3-ol's GND ID is recorded as 4413257-8[5].
  • oct-1-en-3-ol's CAS Registry Number is recorded as 3391-86-4[6].
  • oct-1-en-3-ol's EC number is recorded as 222-226-0[7].
  • oct-1-en-3-ol's canonical SMILES is recorded as CCCCCC(C=C)O[8].
  • oct-1-en-3-ol's InChI is recorded as InChI=1S/C8H16O/c1-3-5-6-7-8(9)4-2/h4,8-9H,2-3,5-7H2,1H3[9].
  • oct-1-en-3-ol's InChIKey is recorded as VSMOENVRRABVKN-UHFFFAOYSA-N[10].
  • oct-1-en-3-ol's chemical formula is recorded as C₈H₁₆O[11].
  • oct-1-en-3-ol's subclass of is recorded as fatty alcohol[12].
  • oct-1-en-3-ol's subclass of is recorded as alkenol[13].
  • oct-1-en-3-ol's Commons category is recorded as 1-Octen-3-ol[14].
  • oct-1-en-3-ol's ChEMBL ID is recorded as CHEMBL3183573[15].
  • oct-1-en-3-ol's Freebase ID is recorded as /m/02z4nbh[16].
  • oct-1-en-3-ol's UNII is recorded as WXB511GE38[17].
  • oct-1-en-3-ol's ChemSpider ID is recorded as 17778[18].
  • oct-1-en-3-ol's PubChem CID is recorded as 18827[19].
  • oct-1-en-3-ol's KEGG ID is recorded as C14272[20].
  • oct-1-en-3-ol's ZVG number is recorded as 40650[21].
  • oct-1-en-3-ol's ChEBI ID is recorded as 34118[22].
  • oct-1-en-3-ol's found in taxon is recorded as Perilla frutescens[23].
  • oct-1-en-3-ol's found in taxon is recorded as Prunus dulcis[24].
  • oct-1-en-3-ol's found in taxon is recorded as Pelargonium graveolens[25].
  • oct-1-en-3-ol's found in taxon is recorded as Thymus quinquecostatus[26].
  • oct-1-en-3-ol's found in taxon is recorded as Dryopteris filix-mas[27].

Why It Matters

oct-1-en-3-ol draws 27 Wikipedia views per month (group_of_stereoisomers category, ranking #191 of 1,063).[2] oct-1-en-3-ol has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] oct-1-en-3-ol is known by 21 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] ↑ . wikidata.org.
  4. [6] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  21. [23] ↑ . Monoterpene biosynthesis by callus tissues and suspension cells from Perilla species. wikidata.org.
  22. [24] ↑ . Components of almond hulls: possible navel orangeworm attractants and growth inhibitors. wikidata.org.
  23. [25] ↑ . (5R*, 9S*)- and (5R*, 9R*)-2,2,9-Trimethyl-1,6-dioxaspiro[4.4]non-3-ene and their Dihydro Derivatives as New Constituents of Geranium Oil. wikidata.org.
  24. [26] ↑ . The Constituents of the Essential Oil from Thymus quinquecostatus Celak.. wikidata.org.
  25. [27] ↑ . Glycosidically Bound Volatile Aliphatic and Aromatic Alcohols—A Common Feature in the Vegetable Kingdom?. 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). oct-1-en-3-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/oct-1-en-3-ol
MLA “oct-1-en-3-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/oct-1-en-3-ol.
BibTeX @misc{4ortxyz_oct-1-en-3-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{oct-1-en-3-ol}}, year = {2026}, url = {https://4ort.xyz/entity/oct-1-en-3-ol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): oct-1-en-3-ol — https://4ort.xyz/entity/oct-1-en-3-ol (retrieved 2026-05-03)

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