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3,4,5-trimethoxyallyl benzene

chemical compound
ChemicalSubstance type_of_chemical_entity Q417746
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3,4,5-trimethoxyallyl benzene

Summary

3,4,5-trimethoxyallyl benzene is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (50 views/month).[2]

Key Facts

  • 3,4,5-trimethoxyallyl benzene's instance of is recorded as type of chemical entity[3].
  • 3,4,5-trimethoxyallyl benzene's chemical structure is recorded as Elemicin.png[4].
  • 3,4,5-trimethoxyallyl benzene's chemical structure is recorded as Elemicin skeletal.svg[5].
  • 3,4,5-trimethoxyallyl benzene's CAS Registry Number is recorded as 487-11-6[6].
  • 3,4,5-trimethoxyallyl benzene's EC number is recorded as 207-649-0[7].
  • 3,4,5-trimethoxyallyl benzene's canonical SMILES is recorded as COC1=CC(=CC(=C1OC)OC)CC=C[8].
  • 3,4,5-trimethoxyallyl benzene's InChI is recorded as InChI=1S/C12H16O3/c1-5-6-9-7-10(13-2)12(15-4)11(8-9)14-3/h5,7-8H,1,6H2,2-4H3[9].
  • 3,4,5-trimethoxyallyl benzene's InChIKey is recorded as BPLQKQKXWHCZSS-UHFFFAOYSA-N[10].
  • 3,4,5-trimethoxyallyl benzene's chemical formula is recorded as C₁₂H₁₆O₃[11].
  • 3,4,5-trimethoxyallyl benzene's subclass of is recorded as chemical compound[12].
  • 3,4,5-trimethoxyallyl benzene's Commons category is recorded as Elemicin[13].
  • 3,4,5-trimethoxyallyl benzene's has part is recorded as carbon[14].
  • 3,4,5-trimethoxyallyl benzene's ChEMBL ID is recorded as CHEMBL458690[15].
  • 3,4,5-trimethoxyallyl benzene's Freebase ID is recorded as /m/092mp6[16].
  • 3,4,5-trimethoxyallyl benzene's UNII is recorded as HSZ191AKAN[17].
  • 3,4,5-trimethoxyallyl benzene's ChemSpider ID is recorded as 9830[18].
  • 3,4,5-trimethoxyallyl benzene's PubChem CID is recorded as 10248[19].
  • 3,4,5-trimethoxyallyl benzene's KEGG ID is recorded as C10451[20].
  • 3,4,5-trimethoxyallyl benzene's ChEBI ID is recorded as 4771[21].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Garcia parviflora[22].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Peperomia circinnata[23].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Ferula communis[24].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Myristica fragrans[25].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Croton nepetifolius[26].
  • 3,4,5-trimethoxyallyl benzene's found in taxon is recorded as Piper auritum[27].

Why It Matters

3,4,5-trimethoxyallyl benzene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (50 views/month).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] It is known by 5 alternative names across languages and contexts.[29]

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] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . Triterpenes from Garcia parviflora. Cytotoxic evaluation of natural and semisynthetic friedelanes.. wikidata.org.
  21. [23] ↑ . The essential oils ofPeperomia pellucida Kunth andP. circinnata Link var.circinnata. wikidata.org.
  22. [24] ↑ . Antibacterial constituents from the rhizomes ofFerula communis. wikidata.org.
  23. [25] ↑ . Nutmeg oil: Identification and quantitation of its most active constituents as inhibitors of platelet aggregation. wikidata.org.
  24. [26] ↑ . Fixed and volatile constituents of Croton aff. nepetifolius. wikidata.org.
  25. [27] ↑ . Safrole, the Main Component of the Essential Oil from Piper auritum of Panama. 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.
  3. [29] ↑ . 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). 3,4,5-trimethoxyallyl benzene. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-4-5-trimethoxyallyl-benzene
MLA “3,4,5-trimethoxyallyl benzene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-4-5-trimethoxyallyl-benzene.
BibTeX @misc{4ortxyz_3-4-5-trimethoxyallyl-benzene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3,4,5-trimethoxyallyl benzene}}, year = {2026}, url = {https://4ort.xyz/entity/3-4-5-trimethoxyallyl-benzene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3,4,5-trimethoxyallyl benzene — https://4ort.xyz/entity/3-4-5-trimethoxyallyl-benzene (retrieved 2026-05-03)

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