cinerolone

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q104253770
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cinerolone

Summary

cinerolone is a group of stereoisomers[1].

Key Facts

  • cinerolone's instance of is recorded as group of stereoisomers[2].
  • cinerolone's chemical structure is recorded as Cinerolone.svg[3].
  • cinerolone's CAS Registry Number is recorded as 17190-74-8[4].
  • cinerolone's canonical SMILES is recorded as O=C1C(=C(C)C(O)C1)CC=CC[5].
  • cinerolone's InChI is recorded as InChI=1S/C10H14O2/c1-3-4-5-8-7(2)9(11)6-10(8)12/h3-4,9,11H,5-6H2,1-2H3/b4-3-[6].
  • cinerolone's InChIKey is recorded as YLKLJBPHNWWPSF-ARJAWSKDSA-N[7].
  • cinerolone's chemical formula is recorded as C₁₀H₁₄O₂[8].
  • cinerolone's subclass of is recorded as cyclohexenes[9].
  • cinerolone's subclass of is recorded as cyclic ketone[10].
  • cinerolone's subclass of is recorded as secondary alcohol[11].
  • cinerolone's subclass of is recorded as olefinic compound[12].
  • cinerolone's PubChem CID is recorded as 5374041[13].
  • cinerolone's found in taxon is recorded as Vaccinium ashei[14].
  • cinerolone's found in taxon is recorded as Vaccinium virgatum[15].
  • cinerolone's found in taxon is recorded as Vaccinium corymbosum[16].
  • cinerolone's found in taxon is recorded as Clinopodium congestum[17].
  • cinerolone's isomeric SMILES is recorded as C/C=C\CC1=C(C(CC1=O)O)C[18].
  • cinerolone's KNApSAcK ID is recorded as C00060341[19].
  • cinerolone's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+166.099379688'}[20].
  • cinerolone's SureChEMBL ID is recorded as 10631200[21].
  • cinerolone's UniChem compound ID is recorded as 66500774[22].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . GLC-MS Analysis of Volatile Constituents in Rabbiteye Blueberries. wikidata.org.
  14. [15] . GLC-MS Analysis of Volatile Constituents in Rabbiteye Blueberries. wikidata.org.
  15. [16] . GLC-MS Analysis of Volatile Constituents in Rabbiteye Blueberries. wikidata.org.
  16. [17] . Composition of the Essential Oil ofMicromeria congesta. wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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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). cinerolone. Retrieved May 3, 2026, from https://4ort.xyz/entity/cinerolone
MLA “cinerolone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cinerolone.
BibTeX @misc{4ortxyz_cinerolone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cinerolone}}, year = {2026}, url = {https://4ort.xyz/entity/cinerolone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cinerolone — https://4ort.xyz/entity/cinerolone (retrieved 2026-05-03)

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