2,6-Dimethyl-3,7-octadiene-2,6-diol

group of stereoisomers with the chemical formula C₁₀H₁₈O₂
ChemicalSubstance group_of_stereoisomers Q115946404
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Summary

2,6-Dimethyl-3,7-octadiene-2,6-diol is a group of stereoisomers[1].

Key Facts

  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's instance of is recorded as group of stereoisomers[2].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's canonical SMILES is recorded as OC(C=CCC(O)(C=C)C)(C)C[3].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's InChI is recorded as InChI=1S/C10H18O2/c1-5-10(4,12)8-6-7-9(2,3)11/h5-7,11-12H,1,8H2,2-4H3/b7-6+[4].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's InChIKey is recorded as QEOHJVNDENHRCH-VOTSOKGWSA-N[5].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's chemical formula is recorded as C₁₀H₁₈O₂[6].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's subclass of is recorded as chemical compound[7].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's PubChem CID is recorded as 5352451[8].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's ChEBI ID is recorded as 180224[9].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's found in taxon is recorded as Artemisia granatensis[10].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's found in taxon is recorded as basil[11].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's isomeric SMILES is recorded as C=CC(C)(O)C/C=C/C(C)(C)O[12].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's Human Metabolome Database ID is recorded as HMDB0036990[13].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's KNApSAcK ID is recorded as C00052671[14].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+170.130679816'}[15].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's SureChEMBL ID is recorded as 942494[16].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's SureChEMBL ID is recorded as 942493[17].
  • 2,6-Dimethyl-3,7-octadiene-2,6-diol's UniChem compound ID is recorded as 32019483[18].

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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Terpenes and polyacetylenes from cultivated Artemisia granatensis boiss (Royal chamomile) and their defensive properties.. wikidata.org.
  10. [11] ↑ . Chemical composition and antioxidant capacity of free volatile aglycones from basil (Ocimum basilicum L.) compared with its essential oil. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 2,6-Dimethyl-3,7-octadiene-2,6-diol. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-6-dimethyl-3-7-octadiene-2-6-diol
MLA “2,6-Dimethyl-3,7-octadiene-2,6-diol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-6-dimethyl-3-7-octadiene-2-6-diol.
BibTeX @misc{4ortxyz_2-6-dimethyl-3-7-octadiene-2-6-diol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2,6-Dimethyl-3,7-octadiene-2,6-diol}}, year = {2026}, url = {https://4ort.xyz/entity/2-6-dimethyl-3-7-octadiene-2-6-diol}, note = {Accessed: 2026-05-03}}
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