β-himachalene

pair of enantiomers
ChemicalSubstance group_of_stereoisomers Q27121533
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β-himachalene

Summary

β-himachalene is a group of stereoisomers[1].

Key Facts

  • β-himachalene's instance of is recorded as group of stereoisomers[2].
  • β-himachalene's CAS Registry Number is recorded as 17928-54-0[3].
  • β-himachalene's canonical SMILES is recorded as CC1=CC2C(=C(CCCC2(C)C)C)CC1[4].
  • β-himachalene's InChI is recorded as InChI=1S/C15H24/c1-11-7-8-13-12(2)6-5-9-15(3,4)14(13)10-11/h10,14H,5-9H2,1-4H3[5].
  • β-himachalene's InChIKey is recorded as LCOSCMLXPAQCLQ-UHFFFAOYSA-N[6].
  • β-himachalene's chemical formula is recorded as C₁₅H₂₄[7].
  • β-himachalene's subclass of is recorded as himachalene[8].
  • β-himachalene's ChemSpider ID is recorded as 14367[9].
  • β-himachalene's PubChem CID is recorded as 15095[10].
  • β-himachalene's ChEBI ID is recorded as 49210[11].
  • β-himachalene's found in taxon is recorded as Curcuma wenyujin[12].
  • β-himachalene's found in taxon is recorded as Curcuma phaeocaulis[13].
  • β-himachalene's found in taxon is recorded as Curcuma kwangsiensis[14].
  • β-himachalene's found in taxon is recorded as Cedrus deodara[15].
  • β-himachalene's found in taxon is recorded as Curcuma zedoaria[16].
  • β-himachalene's found in taxon is recorded as Taxus baccata[17].
  • β-himachalene's found in taxon is recorded as Ambrosia microcephala[18].
  • β-himachalene's found in taxon is recorded as Curcuma aromatica[19].
  • β-himachalene's Reaxys registry number is recorded as 2501577[20].
  • β-himachalene's Human Metabolome Database ID is recorded as HMDB0302863[21].
  • β-himachalene's LIPID MAPS ID is recorded as LMPR0103480005[22].
  • β-himachalene's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+204.188'}[23].
  • β-himachalene's SureChEMBL ID is recorded as 932988[24].
  • β-himachalene's DSSTox substance ID is recorded as DTXSID90932760[25].
  • β-himachalene's DSSTOX compound identifier is recorded as DTXCID701361442[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . SciFinder. wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques. wikidata.org.
  12. [13] ↑ . Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques. wikidata.org.
  13. [14] ↑ . Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques. wikidata.org.
  14. [15] ↑ . Phytochemical analysis and in vitro evaluation of the biological activity against herpes simplex virus type 1 (HSV-1) of Cedrus libani A. Rich. wikidata.org.
  15. [16] ↑ . Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques. wikidata.org.
  16. [17] ↑ . A New Drimane Sesquiterpene, Isomers of Manoyl Oxide and Other Volatile Constituents from the Resin “Ladano” ofCistus incanussubsp.creticus(L.) Heywood. wikidata.org.
  17. [18] ↑ . Essential Oil of Ambrosia microcephala DC. wikidata.org.
  18. [19] ↑ . Metabolite analysis in Curcuma domestica using various GC-MS and LC-MS separation and detection techniques. wikidata.org.
  19. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  22. [23] ↑ . PubChem. Retrieved . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . 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). β-himachalene. Retrieved May 3, 2026, from https://4ort.xyz/entity/-himachalene-q27121533
MLA “β-himachalene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-himachalene-q27121533.
BibTeX @misc{4ortxyz_-himachalene-q27121533_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{β-himachalene}}, year = {2026}, url = {https://4ort.xyz/entity/-himachalene-q27121533}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): β-himachalene — https://4ort.xyz/entity/-himachalene-q27121533 (retrieved 2026-05-03)

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