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2-nonanol

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q4596913
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2-nonanol

Summary

2-nonanol is a group of stereoisomers[1]. 2-nonanol draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #215 of 1,063).[2]

Key Facts

  • 2-nonanol's instance of is recorded as group of stereoisomers[3].
  • 2-nonanol's chemical structure is recorded as 2-Nonanol.svg[4].
  • 2-nonanol's CAS Registry Number is recorded as 628-99-9[5].
  • 2-nonanol's EC number is recorded as 211-065-1[6].
  • 2-nonanol's canonical SMILES is recorded as CCCCCCCC(C)O[7].
  • 2-nonanol's InChI is recorded as InChI=1S/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3[8].
  • 2-nonanol's InChIKey is recorded as NGDNVOAEIVQRFH-UHFFFAOYSA-N[9].
  • 2-nonanol's chemical formula is recorded as C₉H₂₀O[10].
  • 2-nonanol's subclass of is recorded as nonanols[11].
  • 2-nonanol's subclass of is recorded as fatty alcohol[12].
  • 2-nonanol's Commons category is recorded as 2-Nonanol[13].
  • 2-nonanol's ChEMBL ID is recorded as CHEMBL454517[14].
  • 2-nonanol's Freebase ID is recorded as /m/04f2gd0[15].
  • 2-nonanol's UNII is recorded as 292T5234DX[16].
  • 2-nonanol's ChemSpider ID is recorded as 11861[17].
  • 2-nonanol's PubChem CID is recorded as 12367[18].
  • 2-nonanol's ZVG number is recorded as 493573[19].
  • 2-nonanol's ChEBI ID is recorded as 78304[20].
  • 2-nonanol's found in taxon is recorded as Zingiber mioga[21].
  • 2-nonanol's found in taxon is recorded as Camellia sinensis[22].
  • 2-nonanol's found in taxon is recorded as maize[23].
  • 2-nonanol's found in taxon is recorded as ginger[24].
  • 2-nonanol's found in taxon is recorded as Pelargonium endlicherianum[25].
  • 2-nonanol's found in taxon is recorded as Etlingera elatior[26].
  • 2-nonanol's found in taxon is recorded as Ruta angustifolia[27].

Why It Matters

2-nonanol draws 3 Wikipedia views per month (group_of_stereoisomers category, ranking #215 of 1,063).[2] 2-nonanol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] 2-nonanol is known by 10 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . Freebase Data Dumps. wikidata.org.
  14. [16] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . ChEMBL. Retrieved . wikidata.org.
  19. [21] ↑ . Volatile Flavor Compounds of Myoga (Zingiber Mioga).. wikidata.org.
  20. [22] ↑ . Enantiomeric separation of chiral components reported to be in coffee, tea, or cocoa. wikidata.org.
  21. [23] ↑ . Volatiles of corn tassels: possible corn ear worm attractants. wikidata.org.
  22. [24] ↑ . Glycosidically bound aroma compounds in ginger (Zingiber officinale Roscoe). wikidata.org.
  23. [25] ↑ . The analysis of essential oil and headspace volatiles of the flowers of Pelargonium endlicherianum used as an anthelmintic in folk medicine. wikidata.org.
  24. [26] ↑ . The Essential Oil of Young Flower Shoots of Phaeomeria speciosa Koord. wikidata.org.
  25. [27] ↑ . Novel Moskachan Related Compounds in the Essential Oil of Ruta angustifolia Pers. from Malaysia. 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). 2-nonanol. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-nonanol
MLA “2-nonanol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-nonanol.
BibTeX @misc{4ortxyz_2-nonanol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-nonanol}}, year = {2026}, url = {https://4ort.xyz/entity/2-nonanol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 2-nonanol — https://4ort.xyz/entity/2-nonanol (retrieved 2026-05-03)

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