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4-acetylanisole

chemical compound
ChemicalSubstance type_of_chemical_entity Q229995
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4-acetylanisole

Summary

4-acetylanisole is a type of chemical entity[1]. 4-acetylanisole ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2]

Key Facts

  • 4-acetylanisole's instance of is recorded as type of chemical entity[3].
  • 4-acetylanisole's chemical structure is recorded as Acetanisole V.1.svg[4].
  • 4-acetylanisole's chemical structure is recorded as Acetylanisole.png[5].
  • 4-acetylanisole's CAS Registry Number is recorded as 100-06-1[6].
  • 4-acetylanisole's EC number is recorded as 202-815-9[7].
  • 4-acetylanisole's canonical SMILES is recorded as CC(=O)C1=CC=C(C=C1)OC[8].
  • 4-acetylanisole's InChI is recorded as InChI=1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3[9].
  • 4-acetylanisole's InChIKey is recorded as NTPLXRHDUXRPNE-UHFFFAOYSA-N[10].
  • 4-acetylanisole's chemical formula is recorded as C₉H₁₀O₂[11].
  • 4-acetylanisole's subclass of is recorded as chemical compound[12].
  • 4-acetylanisole's Commons category is recorded as Acetanisole[13].
  • 4-acetylanisole's ChEMBL ID is recorded as CHEMBL401912[14].
  • 4-acetylanisole's Freebase ID is recorded as /m/02vnw2r[15].
  • 4-acetylanisole's UNII is recorded as 0IRH2BR587[16].
  • 4-acetylanisole's ChemSpider ID is recorded as 13835344[17].
  • 4-acetylanisole's PubChem CID is recorded as 7476[18].
  • 4-acetylanisole's ChEBI ID is recorded as 86567[19].
  • 4-acetylanisole's found in taxon is recorded as Paeonia lactiflora[20].
  • 4-acetylanisole's found in taxon is recorded as Chuquiraga spinosa[21].
  • 4-acetylanisole's found in taxon is recorded as Tanacetum sinaicum[22].
  • 4-acetylanisole's found in taxon is recorded as Aronia melanocarpa[23].
  • 4-acetylanisole's found in taxon is recorded as Mitracarpus hirtus[24].
  • 4-acetylanisole's found in taxon is recorded as Pulicaria paludosa[25].
  • 4-acetylanisole's found in taxon is recorded as Scutellaria baicalensis[26].
  • 4-acetylanisole's found in taxon is recorded as Foeniculum vulgare[27].

Why It Matters

4-acetylanisole ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (18 views/month).[2] 4-acetylanisole has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[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] ↑ . wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . Freebase Data Dumps. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  18. [20] ↑ . "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.).". wikidata.org.
  19. [21] ↑ . Composition of the Essential Oil ofChuquiraga spinosa (R. et P.) D. Don. wikidata.org.
  20. [22] ↑ . Sesquiterpene lactones from Pyrethrum santolinoides. wikidata.org.
  21. [23] ↑ . Analysis of the volatile constituents of black chokeberry (Aronia melanocarpa Ell.). wikidata.org.
  22. [24] ↑ . Antimicrobial activity of Mitracarpus scaber extract and isolated constituents.. wikidata.org.
  23. [25] ↑ . The Structures of Pulicaral and Related Sesquiterpenoids from Pulicaria paludosa. wikidata.org.
  24. [26] ↑ . Essential oil of Scutellaria baicalensis G.. wikidata.org.
  25. [27] ↑ . Headspace solvent microextraction-gas chromatography-mass spectrometry for the analysis of volatile compounds from Foeniculum vulgare Mill. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. 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). 4-acetylanisole. Retrieved May 3, 2026, from https://4ort.xyz/entity/4-acetylanisole
MLA “4-acetylanisole.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/4-acetylanisole.
BibTeX @misc{4ortxyz_4-acetylanisole_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{4-acetylanisole}}, year = {2026}, url = {https://4ort.xyz/entity/4-acetylanisole}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 4-acetylanisole — https://4ort.xyz/entity/4-acetylanisole (retrieved 2026-05-03)

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