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(E)-5-methyl-2-hepten-4-one

chemical compound
ChemicalSubstance group_of_stereoisomers Q5448299
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(E)-5-methyl-2-hepten-4-one

Summary

(E)-5-methyl-2-hepten-4-one is a group of stereoisomers[1]. (E)-5-methyl-2-hepten-4-one draws 27 Wikipedia views per month (group_of_stereoisomers category, ranking #202 of 1,063).[2]

Key Facts

  • (E)-5-methyl-2-hepten-4-one's instance of is recorded as group of stereoisomers[3].
  • (E)-5-methyl-2-hepten-4-one's chemical structure is recorded as Filbertone.svg[4].
  • (E)-5-methyl-2-hepten-4-one's CAS Registry Number is recorded as 102322-83-8[5].
  • (E)-5-methyl-2-hepten-4-one's EC number is recorded as 600-299-3[6].
  • (E)-5-methyl-2-hepten-4-one's canonical SMILES is recorded as CCC(C)C(=O)C=CC[7].
  • (E)-5-methyl-2-hepten-4-one's InChI is recorded as InChI=1S/C8H14O/c1-4-6-8(9)7(3)5-2/h4,6-7H,5H2,1-3H3/b6-4+[8].
  • (E)-5-methyl-2-hepten-4-one's InChIKey is recorded as ARJWAURHQDJJAC-GQCTYLIASA-N[9].
  • (E)-5-methyl-2-hepten-4-one's chemical formula is recorded as C₈H₁₄O[10].
  • (E)-5-methyl-2-hepten-4-one's subclass of is recorded as biogenic acyclic ketone[11].
  • (E)-5-methyl-2-hepten-4-one's subclass of is recorded as 5-methyl-2-hepten-4-one[12].
  • (E)-5-methyl-2-hepten-4-one's has use is recorded as aroma compound[13].
  • (E)-5-methyl-2-hepten-4-one's Commons category is recorded as Filbertone[14].
  • (E)-5-methyl-2-hepten-4-one's Freebase ID is recorded as /m/0nd4jkk[15].
  • (E)-5-methyl-2-hepten-4-one's UNII is recorded as 8K2S58736F[16].
  • (E)-5-methyl-2-hepten-4-one's ChemSpider ID is recorded as 4515100[17].
  • (E)-5-methyl-2-hepten-4-one's PubChem CID is recorded as 5362588[18].
  • (E)-5-methyl-2-hepten-4-one's found in taxon is recorded as Corylus avellana[19].
  • (E)-5-methyl-2-hepten-4-one's isomeric SMILES is recorded as CCC(C)C(=O)/C=C/C[20].
  • (E)-5-methyl-2-hepten-4-one's Human Metabolome Database ID is recorded as HMDB0303507[21].
  • (E)-5-methyl-2-hepten-4-one's mass is recorded as {'unit': 'Q483261', 'amount': '+126.104'}[22].
  • (E)-5-methyl-2-hepten-4-one's ECHA Substance Infocard ID is recorded as 100.133.148[23].
  • (E)-5-methyl-2-hepten-4-one's SureChEMBL ID is recorded as 310232[24].
  • (E)-5-methyl-2-hepten-4-one's CosIng number is recorded as 40689[25].
  • (E)-5-methyl-2-hepten-4-one's DSSTox substance ID is recorded as DTXSID401017670[26].
  • (E)-5-methyl-2-hepten-4-one's Microsoft Academic ID is recorded as 2779922079[27].

Why It Matters

(E)-5-methyl-2-hepten-4-one draws 27 Wikipedia views per month (group_of_stereoisomers category, ranking #202 of 1,063).[2] (E)-5-methyl-2-hepten-4-one is known by 3 alternative names across languages and contexts.[28]

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] ↑ . ECHA Substance Infocard database. 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] ↑ . wikidata.org.
  14. [16] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . Isolation, Synthesis, and Absolute Configuration of Filbertone - the Principal Flavor Component of the Hazelnut. wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata aliases. wikidata.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). (E)-5-methyl-2-hepten-4-one. Retrieved May 3, 2026, from https://4ort.xyz/entity/e-5-methyl-2-hepten-4-one
MLA “(E)-5-methyl-2-hepten-4-one.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/e-5-methyl-2-hepten-4-one.
BibTeX @misc{4ortxyz_e-5-methyl-2-hepten-4-one_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(E)-5-methyl-2-hepten-4-one}}, year = {2026}, url = {https://4ort.xyz/entity/e-5-methyl-2-hepten-4-one}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (E)-5-methyl-2-hepten-4-one — https://4ort.xyz/entity/e-5-methyl-2-hepten-4-one (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. 5w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Has use → aroma compound
    Instance of → group of stereoisomers
    Subclass of → biogenic acyclic ketone, 5-methyl-2-hepten-4-one
    Found in taxon → Corylus avellana
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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