methyl anisate

chemical compound
ChemicalSubstance type_of_chemical_entity Q6823933
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Summary

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

Key Facts

  • methyl anisate's instance of is recorded as type of chemical entity[3].
  • methyl anisate's chemical structure is recorded as Methyl anisate.svg[4].
  • methyl anisate's CAS Registry Number is recorded as 121-98-2[5].
  • methyl anisate's EC number is recorded as 204-513-2[6].
  • methyl anisate's canonical SMILES is recorded as COC1=CC=C(C=C1)C(=O)OC[7].
  • methyl anisate's InChI is recorded as InChI=1S/C9H10O3/c1-11-8-5-3-7(4-6-8)9(10)12-2/h3-6H,1-2H3[8].
  • methyl anisate's InChIKey is recorded as DDIZAANNODHTRB-UHFFFAOYSA-N[9].
  • methyl anisate's chemical formula is recorded as C₉H₁₀O₃[10].
  • methyl anisate's subclass of is recorded as parabens[11].
  • methyl anisate's ChEMBL ID is recorded as CHEMBL1762668[12].
  • methyl anisate's Freebase ID is recorded as /m/0j642ct[13].
  • methyl anisate's UNII is recorded as 2MFL7873W9[14].
  • methyl anisate's ChemSpider ID is recorded as 21108577[15].
  • methyl anisate's PubChem CID is recorded as 8499[16].
  • methyl anisate's ChEBI ID is recorded as 86903[17].
  • methyl anisate's found in taxon is recorded as Illicium verum[18].
  • methyl anisate's found in taxon is recorded as Polygala senega[19].
  • methyl anisate's found in taxon is recorded as Paeonia lactiflora[20].
  • methyl anisate's found in taxon is recorded as Hydnellum suaveolens[21].
  • methyl anisate's found in taxon is recorded as Mycobacterium bovis[22].
  • methyl anisate's found in taxon is recorded as Mycobacterium tuberculosis[23].
  • methyl anisate's found in taxon is recorded as Phellodendron amurense[24].
  • methyl anisate's found in taxon is recorded as Annona cherimola[25].
  • methyl anisate's found in taxon is recorded as Acca sellowiana[26].
  • methyl anisate's found in taxon is recorded as Foeniculum vulgare[27].

Why It Matters

methyl anisate ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (4 views/month).[2] It is known by 5 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] ↑ . 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] ↑ . ChemSpider. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . GC/MS Analysis of Star Anise Oil. wikidata.org.
  17. [19] ↑ . Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots. wikidata.org.
  18. [20] ↑ . Volatile constituents of peony flowers. wikidata.org.
  19. [21] ↑ . The Identity and Metabolic Fate of Volatiles Responsible for the Odor of Hydnellum suaveolens. wikidata.org.
  20. [22] ↑ . The scent of Mycobacterium tuberculosis.. wikidata.org.
  21. [23] ↑ . The scent of Mycobacterium tuberculosis.. wikidata.org.
  22. [24] ↑ . Constituents from the leaves of Phellodendron amurense and their antioxidant activity. wikidata.org.
  23. [25] ↑ . Annocherine C, A New C-α Hydroxy Benzylisoquinoline and Other Constituents from the Leaves ofAnnona Cherimola. wikidata.org.
  24. [26] ↑ . Volatile components of feijoa fruits. wikidata.org.
  25. [27] ↑ . Inhibition on human liver cytochrome P450 3A4 by constituents of fennel (Foeniculum vulgare): identification and characterization of a mechanism-based inactivator. 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). methyl anisate. Retrieved October 14, 2026, from https://4ort.xyz/entity/methyl-anisate
MLA “methyl anisate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 14 Oct. 2026, https://4ort.xyz/entity/methyl-anisate.
BibTeX @misc{4ortxyz_methyl-anisate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{methyl anisate}}, year = {2026}, url = {https://4ort.xyz/entity/methyl-anisate}, note = {Accessed: 2026-10-14}}
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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. 23w ago · KaleemBot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of → parabens
    Found in taxon → Illicium verum, Polygala senega, Paeonia lactiflora +9
    Mass → {'unit': 'Q483261', 'amount': '+166.063'}
    Instance of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:میتھائل اینیسیٹ]]"
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