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(+/-)-lavandulyl acetate

chemical compound
ChemicalSubstance group_of_stereoisomers Q16948466
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(+/-)-lavandulyl acetate

Summary

(+/-)-lavandulyl acetate is a group of stereoisomers[1]. (+/-)-lavandulyl acetate draws 2 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]

Key Facts

  • (+/-)-lavandulyl acetate's instance of is recorded as group of stereoisomers[3].
  • (+/-)-lavandulyl acetate's chemical structure is recorded as Lavandulyl acetate.svg[4].
  • (+/-)-lavandulyl acetate's CAS Registry Number is recorded as 25905-14-0[5].
  • (+/-)-lavandulyl acetate's EC number is recorded as 247-327-7[6].
  • (+/-)-lavandulyl acetate's canonical SMILES is recorded as CC(=CCC(COC(=O)C)C(=C)C)C[7].
  • (+/-)-lavandulyl acetate's InChI is recorded as InChI=1S/C12H20O2/c1-9(2)6-7-12(10(3)4)8-14-11(5)13/h6,12H,3,7-8H2,1-2,4-5H3[8].
  • (+/-)-lavandulyl acetate's InChIKey is recorded as HYNGAVZPWWXQIU-UHFFFAOYSA-N[9].
  • (+/-)-lavandulyl acetate's chemical formula is recorded as C₁₂H₂₀O₂[10].
  • (+/-)-lavandulyl acetate's subclass of is recorded as 2,3,6-trimethylheptane monoterpenoid[11].
  • (+/-)-lavandulyl acetate's subclass of is recorded as biogenic acyclic ester[12].
  • (+/-)-lavandulyl acetate's Commons category is recorded as Lavandulyl acetate[13].
  • (+/-)-lavandulyl acetate's Freebase ID is recorded as /m/0_v9h9d[14].
  • (+/-)-lavandulyl acetate's UNII is recorded as OU6ZF37MOM[15].
  • (+/-)-lavandulyl acetate's ChemSpider ID is recorded as 28088[16].
  • (+/-)-lavandulyl acetate's PubChem CID is recorded as 30247[17].
  • (+/-)-lavandulyl acetate's found in taxon is recorded as Alpinia galanga[18].
  • (+/-)-lavandulyl acetate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+196.146'}[19].
  • (+/-)-lavandulyl acetate's ECHA Substance Infocard ID is recorded as 100.043.010[20].
  • (+/-)-lavandulyl acetate's SureChEMBL ID is recorded as 132576[21].
  • (+/-)-lavandulyl acetate's CosIng number is recorded as 40373[22].
  • (+/-)-lavandulyl acetate's DSSTox substance ID is recorded as DTXSID6051932[23].
  • (+/-)-lavandulyl acetate's DSSTox substance ID is recorded as DTXSID30904865[24].
  • (+/-)-lavandulyl acetate's Microsoft Academic ID is recorded as 2781339017[25].
  • (+/-)-lavandulyl acetate's DSSTOX compound identifier is recorded as DTXCID501333982[26].
  • (+/-)-lavandulyl acetate's FL number is recorded as 09.612[27].

Why It Matters

(+/-)-lavandulyl acetate draws 2 Wikipedia views per month (group_of_stereoisomers category, ranking #216 of 1,063).[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . Chemical composition, antifeedant, repellent, and toxicity activities of the rhizomes of galangal, Alpinia galanga against Asian subterranean termites, Coptotermes gestroi and Coptotermes curvignathus (Isoptera: Rhinotermitidae).. wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . CosIng database. Retrieved . wikidata.org.
  21. [23] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . EFSA database. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.

📑 Cite this page

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). (+/-)-lavandulyl acetate. Retrieved May 3, 2026, from https://4ort.xyz/entity/-lavandulyl-acetate
MLA “(+/-)-lavandulyl acetate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-lavandulyl-acetate.
BibTeX @misc{4ortxyz_-lavandulyl-acetate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+/-)-lavandulyl acetate}}, year = {2026}, url = {https://4ort.xyz/entity/-lavandulyl-acetate}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+/-)-lavandulyl acetate — https://4ort.xyz/entity/-lavandulyl-acetate (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 19w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Freebase id → /m/0_v9h9d
    Canonical smiles → CC(=CCC(COC(=O)C)C(=C)C)C
    Pubchem cid → 30247
    Wikidata description → chemical compound
    + 22 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.