(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol

group of stereoisomers with the chemical formula C₁₅H₂₆O
ChemicalSubstance group_of_stereoisomers Q104667242
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(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol

Summary

(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol is a group of stereoisomers[1].

Key Facts

  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's instance of is recorded as group of stereoisomers[2].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's canonical SMILES is recorded as OC1(C)CCC(C(C)C)C2C=C(C)CCC21[3].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's InChI is recorded as InChI=1S/C15H26O/c1-10(2)12-7-8-15(4,16)14-6-5-11(3)9-13(12)14/h9-10,12-14,16H,5-8H2,1-4H3/t12?,13-,14-,15+/m0/s1[4].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's InChIKey is recorded as LHYHMMRYTDARSZ-WIGRTHMWSA-N[5].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's chemical formula is recorded as C₁₅H₂₆O[6].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's subclass of is recorded as cadinane sesquiterpenoid[7].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's PubChem CID is recorded as 5315594[8].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's found in taxon is recorded as Erigeron canadensis[9].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's found in taxon is recorded as Salvia tomentosa[10].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's found in taxon is recorded as Salvia officinalis[11].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's found in taxon is recorded as Humulus lupulus[12].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's found in taxon is recorded as Eucalyptus[13].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's isomeric SMILES is recorded as CC1=C[C@H]2C(C(C)C)CCC@@(O)[C@H]2CC1C@@(O)[C@H]2CC1">[14].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+222.198365452'}[15].
  • (1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol's UniChem compound ID is recorded as 62856658[16].

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] . The Essential Oil of Erigeron canadensis L.. wikidata.org.
  9. [10] . Constituents of Essential Oils from ThreeSalviaSpecies. wikidata.org.
  10. [11] . Constituents of Essential Oils from ThreeSalviaSpecies. wikidata.org.
  11. [12] . Direct thermal desorption-gas chromatography and gas chromatography-mass spectrometry profiling of hop (Humulus lupulus L.) essential oils in support of varietal characterization. wikidata.org.
  12. [13] . Volatile leaf oils of some South-western and Southern Australian species of the genus Eucalyptus part VI—subgenus symphyomyrtus, section adnataria. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . UniChem. wikidata.org.

Class ancestry

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

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BibTeX @misc{4ortxyz_-1r-4ar-8as-1-6-dimethyl-4-propan-2-yl-3-4-4a-7-8-8a-hexahydro-2h-naphthalen-1-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol}}, year = {2026}, url = {https://4ort.xyz/entity/-1r-4ar-8as-1-6-dimethyl-4-propan-2-yl-3-4-4a-7-8-8a-hexahydro-2h-naphthalen-1-ol}, note = {Accessed: 2026-05-03}}
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