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p-menth-6-ene-2,8-diol

group of stereoisomers with the chemical formula C₁₀H₁₈O₂
ChemicalSubstance group_of_stereoisomers Q105194289
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Summary

p-menth-6-ene-2,8-diol is a group of stereoisomers[1].

Key Facts

  • p-menth-6-ene-2,8-diol's instance of is recorded as group of stereoisomers[2].
  • p-menth-6-ene-2,8-diol's chemical structure is recorded as Sobrerol.svg[3].
  • p-menth-6-ene-2,8-diol's CAS Registry Number is recorded as 498-71-5[4].
  • p-menth-6-ene-2,8-diol's canonical SMILES is recorded as OC1C(=CCC(C1)C(O)(C)C)C[5].
  • p-menth-6-ene-2,8-diol's InChI is recorded as InChI=1S/C10H18O2/c1-7-4-5-8(6-9(7)11)10(2,3)12/h4,8-9,11-12H,5-6H2,1-3H3[6].
  • p-menth-6-ene-2,8-diol's InChIKey is recorded as OMDMTHRBGUBUCO-UHFFFAOYSA-N[7].
  • p-menth-6-ene-2,8-diol's chemical formula is recorded as C₁₀H₁₈O₂[8].
  • p-menth-6-ene-2,8-diol's subclass of is recorded as menthane monoterpenoids[9].
  • p-menth-6-ene-2,8-diol's PubChem CID is recorded as 91463[10].
  • p-menth-6-ene-2,8-diol's ChEBI ID is recorded as 134802[11].
  • p-menth-6-ene-2,8-diol's found in taxon is recorded as Cyperus[12].
  • p-menth-6-ene-2,8-diol's found in taxon is recorded as Mangifera indica[13].
  • p-menth-6-ene-2,8-diol's Human Metabolome Database ID is recorded as HMDB0258357[14].
  • p-menth-6-ene-2,8-diol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+170.130679816'}[15].
  • p-menth-6-ene-2,8-diol's SureChEMBL ID is recorded as 1649171[16].
  • p-menth-6-ene-2,8-diol's DSSTox substance ID is recorded as DTXSID90871701[17].
  • p-menth-6-ene-2,8-diol's UniChem compound ID is recorded as 26805315[18].
  • p-menth-6-ene-2,8-diol's DrugCentral ID is recorded as 2454[19].
  • p-menth-6-ene-2,8-diol's Probes And Drugs ID is recorded as PD073803[20].

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] ↑ . Chemical Abstracts Service. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI release 2021-03-01. wikidata.org.
  11. [12] ↑ . Structures of new sesquiterpenes and hepatoprotective constituents from the Egyptian herbal medicine Cyperus longus.. wikidata.org.
  12. [13] ↑ . Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.
  19. [20] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). p-menth-6-ene-2,8-diol. Retrieved May 3, 2026, from https://4ort.xyz/entity/p-menth-6-ene-2-8-diol
MLA “p-menth-6-ene-2,8-diol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/p-menth-6-ene-2-8-diol.
BibTeX @misc{4ortxyz_p-menth-6-ene-2-8-diol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{p-menth-6-ene-2,8-diol}}, year = {2026}, url = {https://4ort.xyz/entity/p-menth-6-ene-2-8-diol}, note = {Accessed: 2026-05-03}}
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