trans-ocimenol

chemical compound
ChemicalSubstance group_of_stereoisomers Q82864070
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trans-ocimenol

Summary

trans-ocimenol is a group of stereoisomers[1].

Key Facts

  • trans-ocimenol's instance of is recorded as group of stereoisomers[2].
  • trans-ocimenol's CAS Registry Number is recorded as 28977-58-4[3].
  • trans-ocimenol's canonical SMILES is recorded as CC(=C)C(CC=C(C)C=C)O[4].
  • trans-ocimenol's InChI is recorded as InChI=1S/C10H16O/c1-5-9(4)6-7-10(11)8(2)3/h5-6,10-11H,1-2,7H2,3-4H3/b9-6+[5].
  • trans-ocimenol's InChIKey is recorded as TYDDWHVJHGIJCW-RMKNXTFCSA-N[6].
  • trans-ocimenol's chemical formula is recorded as C₁₀H₁₆O[7].
  • trans-ocimenol's subclass of is recorded as chemical compound[8].
  • trans-ocimenol's UNII is recorded as RD4TJJ74P3[9].
  • trans-ocimenol's PubChem CID is recorded as 5362854[10].
  • trans-ocimenol's found in taxon is recorded as Acca sellowiana[11].
  • trans-ocimenol's found in taxon is recorded as Citrus reticulata[12].
  • trans-ocimenol's found in taxon is recorded as Curcuma mangga[13].
  • trans-ocimenol's found in taxon is recorded as Citrus × deliciosa[14].
  • trans-ocimenol's isomeric SMILES is recorded as CC(=C)C(C/C=C(\C)/C=C)O[15].
  • trans-ocimenol's KNApSAcK ID is recorded as C00056026[16].
  • trans-ocimenol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+152.120115132'}[17].
  • trans-ocimenol's SureChEMBL ID is recorded as 17627633[18].
  • trans-ocimenol's DSSTox substance ID is recorded as DTXSID30885443[19].
  • trans-ocimenol's DSSTOX compound identifier is recorded as DTXCID601024823[20].
  • trans-ocimenol's UniChem compound ID is recorded as 42419967[21].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: 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] . PubChem. Retrieved . wikidata.org.
  10. [11] . Compositional Analysis and Aroma Evaluation of Feijoa Essential Oils from New Zealand Grown Cultivars. wikidata.org.
  11. [12] . Identification and Characterization of Constituents in Si-Wu-Tang by Liquid Chromatography Connected with Time of Flight Mass Spectrometry and Ion Trap Mass Spectrometry. wikidata.org.
  12. [13] . Volatiles of Curcuma manggaVal. & Zijp (Zingiberaceae) from Malaysia. wikidata.org.
  13. [14] . Identification and Characterization of Constituents in Si-Wu-Tang by Liquid Chromatography Connected with Time of Flight Mass Spectrometry and Ion Trap Mass Spectrometry. wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . 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). trans-ocimenol. Retrieved May 3, 2026, from https://4ort.xyz/entity/trans-ocimenol
MLA “trans-ocimenol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trans-ocimenol.
BibTeX @misc{4ortxyz_trans-ocimenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trans-ocimenol}}, year = {2026}, url = {https://4ort.xyz/entity/trans-ocimenol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trans-ocimenol — https://4ort.xyz/entity/trans-ocimenol (retrieved 2026-05-03)

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