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(±)-isobornyl acetate

chemical compound
ChemicalSubstance type_of_chemical_entity Q425010
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(±)-isobornyl acetate

Summary

(±)-isobornyl acetate is a type of chemical entity[1]. (±)-isobornyl acetate ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

Key Facts

  • (±)-isobornyl acetate's instance of is recorded as type of chemical entity[3].
  • (±)-isobornyl acetate's chemical structure is recorded as Isobornyl acetate.svg[4].
  • (±)-isobornyl acetate's chemical structure is recorded as Isobornylacetat.svg[5].
  • (±)-isobornyl acetate's CAS Registry Number is recorded as 125-12-2[6].
  • (±)-isobornyl acetate's EC number is recorded as 204-727-6[7].
  • (±)-isobornyl acetate's canonical SMILES is recorded as CC(=O)OC1CC2CCC1(C2(C)C)C[8].
  • (±)-isobornyl acetate's InChI is recorded as InChI=1S/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10-,12+/m1/s1[9].
  • (±)-isobornyl acetate's InChIKey is recorded as KGEKLUUHTZCSIP-FOGDFJRCSA-N[10].
  • (±)-isobornyl acetate's chemical formula is recorded as C₁₂H₂₀O₂[11].
  • (±)-isobornyl acetate's subclass of is recorded as camphan monoterpenoid[12].
  • (±)-isobornyl acetate's Commons category is recorded as Isobornyl acetate[13].
  • (±)-isobornyl acetate's has part is recorded as carbon[14].
  • (±)-isobornyl acetate's ChEMBL ID is recorded as CHEMBL3183823[15].
  • (±)-isobornyl acetate's UNII is recorded as 54T6CCU09Z[16].
  • (±)-isobornyl acetate's ChemSpider ID is recorded as 553137[17].
  • (±)-isobornyl acetate's PubChem CID is recorded as 637531[18].
  • (±)-isobornyl acetate's ZVG number is recorded as 491983[19].
  • (±)-isobornyl acetate's found in taxon is recorded as Daucus carota[20].
  • (±)-isobornyl acetate's found in taxon is recorded as Lindera aggregata[21].
  • (±)-isobornyl acetate's found in taxon is recorded as Santolina chamaecyparissus[22].
  • (±)-isobornyl acetate's found in taxon is recorded as Santolina villosa[23].
  • (±)-isobornyl acetate's found in taxon is recorded as Chrysanthemum indicum[24].
  • (±)-isobornyl acetate's found in taxon is recorded as Dendranthema indicum[25].
  • (±)-isobornyl acetate's isomeric SMILES is recorded as CC(=O)O[C@@H]1C[C@H]2CC[C@@]1(C2(C)C)C[26].
  • (±)-isobornyl acetate's HSDB ID is recorded as 8452[27].

Why It Matters

(±)-isobornyl acetate ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2] (±)-isobornyl acetate has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

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] ↑ . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  5. [7] ↑ . Global Substance Registration System. 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] ↑ . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Genetic variation for volatile terpenoids in roots of carrot, Daucus carota, inbreds and F1 hybrids. wikidata.org.
  19. [21] ↑ . On terpenes. CXXXV. Composition of the oil from Lindera strychnifolia (F.) WILL. leaves. wikidata.org.
  20. [22] ↑ . Sesquiterpenes from Santolina chamaecyparissus subsp. squarrosa. wikidata.org.
  21. [23] ↑ . Sesquiterpenes from Santolina chamaecyparissus subsp. squarrosa. wikidata.org.
  22. [24] ↑ . Identification of Floral Scent in Chrysanthemum Cultivars and Wild Relatives by Gas Chromatography-Mass Spectrometry. wikidata.org.
  23. [25] ↑ . Identification of Floral Scent in Chrysanthemum Cultivars and Wild Relatives by Gas Chromatography-Mass Spectrometry. wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . Hazardous Substances Data Bank. Retrieved . 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.

📑 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). (±)-isobornyl acetate. Retrieved May 3, 2026, from https://4ort.xyz/entity/isobornyl-acetate
MLA “(±)-isobornyl acetate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/isobornyl-acetate.
BibTeX @misc{4ortxyz_isobornyl-acetate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(±)-isobornyl acetate}}, year = {2026}, url = {https://4ort.xyz/entity/isobornyl-acetate}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (±)-isobornyl acetate — https://4ort.xyz/entity/isobornyl-acetate (retrieved 2026-05-03)

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