acetonylacetone

chemical compound
ChemicalSubstance type_of_chemical_entity Q209264
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acetonylacetone

Summary

acetonylacetone is a type of chemical entity[1]. acetonylacetone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • acetonylacetone's instance of is recorded as type of chemical entity[3].
  • acetonylacetone's chemical structure is recorded as Hexane-2,5-dione-2D-skeletal.svg[4].
  • acetonylacetone's CAS Registry Number is recorded as 110-13-4[5].
  • acetonylacetone's EC number is recorded as 203-738-3[6].
  • acetonylacetone's canonical SMILES is recorded as CC(=O)CCC(=O)C[7].
  • acetonylacetone's InChI is recorded as InChI=1S/C6H10O2/c1-5(7)3-4-6(2)8/h3-4H2,1-2H3[8].
  • acetonylacetone's InChIKey is recorded as OJVAMHKKJGICOG-UHFFFAOYSA-N[9].
  • acetonylacetone's chemical formula is recorded as C₆H₁₀O₂[10].
  • acetonylacetone's subclass of is recorded as oxygenated hydrocarbon[11].
  • acetonylacetone's subclass of is recorded as biogenic acyclic ketone[12].
  • acetonylacetone's Commons category is recorded as Hexane-2,5-dione[13].
  • acetonylacetone's MeSH descriptor ID is recorded as C011269[14].
  • acetonylacetone's ChEMBL ID is recorded as CHEMBL1564795[15].
  • acetonylacetone's Freebase ID is recorded as /m/027hncn[16].
  • acetonylacetone's UNII is recorded as C0Z8884J3P[17].
  • acetonylacetone's RTECS number is recorded as MO3150000[18].
  • acetonylacetone's ChemSpider ID is recorded as 7744[19].
  • acetonylacetone's PubChem CID is recorded as 8035[20].
  • acetonylacetone's ZVG number is recorded as 33830[21].
  • acetonylacetone's ChEBI ID is recorded as 85014[22].
  • acetonylacetone's found in taxon is recorded as Mangifera indica[23].
  • acetonylacetone's found in taxon is recorded as Nicotiana tabacum[24].
  • acetonylacetone's found in taxon is recorded as Magnolia obovata[25].
  • acetonylacetone's described by source is recorded as Armenian Soviet Encyclopedia, vol. 7[26].
  • acetonylacetone's Reaxys registry number is recorded as 506525[27].

Why It Matters

acetonylacetone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] acetonylacetone has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] acetonylacetone 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] . LIPID MAPS. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Medical Subject Headings. Retrieved . wikidata.org.
  13. [15] . ChEMBL. Retrieved . wikidata.org.
  14. [16] . Freebase Data Dumps. wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Q2311683. Retrieved . wikidata.org.
  18. [20] . PubChem. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . ChEMBL. Retrieved . wikidata.org.
  21. [23] . Volatile components from mango (Mangifera indica L.) cultivars. wikidata.org.
  22. [24] . Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves. wikidata.org.
  23. [25] . Composition of the Bark Oil of Magnolia obovata Thunb.. wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . ChEBI. 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.
  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). acetonylacetone. Retrieved May 3, 2026, from https://4ort.xyz/entity/acetonylacetone
MLA “acetonylacetone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/acetonylacetone.
BibTeX @misc{4ortxyz_acetonylacetone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{acetonylacetone}}, year = {2026}, url = {https://4ort.xyz/entity/acetonylacetone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): acetonylacetone — https://4ort.xyz/entity/acetonylacetone (retrieved 2026-05-03)

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