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benzyl cinnamate (trans)

chemical compound
ChemicalSubstance type_of_chemical_entity Q9197460
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benzyl cinnamate (trans)

Summary

benzyl cinnamate (trans) is a type of chemical entity[1]. benzyl cinnamate (trans) ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • benzyl cinnamate (trans)'s instance of is recorded as type of chemical entity[3].
  • benzyl cinnamate (trans)'s chemical structure is recorded as Benzyl cinnamate.svg[4].
  • benzyl cinnamate (trans)'s CAS Registry Number is recorded as 103-41-3[5].
  • benzyl cinnamate (trans)'s EC number is recorded as 203-109-3[6].
  • benzyl cinnamate (trans)'s canonical SMILES is recorded as C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2[7].
  • benzyl cinnamate (trans)'s InChI is recorded as InChI=1S/C16H14O2/c17-16(12-11-14-7-3-1-4-8-14)18-13-15-9-5-2-6-10-15/h1-12H,13H2/b12-11+[8].
  • benzyl cinnamate (trans)'s InChIKey is recorded as NGHOLYJTSCBCGC-VAWYXSNFSA-N[9].
  • benzyl cinnamate (trans)'s chemical formula is recorded as C₁₆H₁₄O₂[10].
  • benzyl cinnamate (trans)'s subclass of is recorded as benzyl cinnamate[11].
  • benzyl cinnamate (trans)'s Commons category is recorded as Benzyl cinnamate[12].
  • benzyl cinnamate (trans)'s ChEMBL ID is recorded as CHEMBL361197[13].
  • benzyl cinnamate (trans)'s Freebase ID is recorded as /m/0_s3h3b[14].
  • benzyl cinnamate (trans)'s UNII is recorded as V67O3RO97U[15].
  • benzyl cinnamate (trans)'s ChemSpider ID is recorded as 4437893[16].
  • benzyl cinnamate (trans)'s PubChem CID is recorded as 5273469[17].
  • benzyl cinnamate (trans)'s ZVG number is recorded as 492647[18].
  • benzyl cinnamate (trans)'s ChEBI ID is recorded as 146174[19].
  • benzyl cinnamate (trans)'s found in taxon is recorded as Tephrosia sinapou[20].
  • benzyl cinnamate (trans)'s found in taxon is recorded as Balantiopsis rosea[21].
  • benzyl cinnamate (trans)'s found in taxon is recorded as Isotachis japonica[22].
  • benzyl cinnamate (trans)'s found in taxon is recorded as Friesodielsia velutina[23].
  • benzyl cinnamate (trans)'s isomeric SMILES is recorded as C1=CC=C(C=C1)COC(=O)/C=C/C2=CC=CC=C2[24].
  • benzyl cinnamate (trans)'s HSDB ID is recorded as 359[25].
  • benzyl cinnamate (trans)'s KNApSAcK ID is recorded as C00019222[26].
  • benzyl cinnamate (trans)'s KNApSAcK ID is recorded as C00058958[27].

Why It Matters

benzyl cinnamate (trans) ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] benzyl cinnamate (trans) has Wikipedia articles in 5 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] ↑ . Global Substance Registration System. Retrieved . 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] ↑ . ChEMBL. Retrieved . 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] ↑ . wikidata.org.
  17. [19] ↑ . ChEBI release 2021-03-01. wikidata.org.
  18. [20] ↑ . Potential cancer chemopreventive flavonoids from the stems of Tephrosia toxicaria. wikidata.org.
  19. [21] ↑ . Isotachin c and balantiolide two aromatic compounds from the new zealand liverwort balantiopsis rosea. wikidata.org.
  20. [22] ↑ . Isotachin c and balantiolide two aromatic compounds from the new zealand liverwort balantiopsis rosea. wikidata.org.
  21. [23] ↑ . Alkaloids, flavonoids and phenylpropanoids of the west African plant Oxymitra velutina. wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . Hazardous Substances Data Bank. Retrieved . 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 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). benzyl cinnamate (trans). Retrieved May 3, 2026, from https://4ort.xyz/entity/benzyl-cinnamate-trans
MLA “benzyl cinnamate (trans).” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/benzyl-cinnamate-trans.
BibTeX @misc{4ortxyz_benzyl-cinnamate-trans_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{benzyl cinnamate (trans)}}, year = {2026}, url = {https://4ort.xyz/entity/benzyl-cinnamate-trans}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): benzyl cinnamate (trans) — https://4ort.xyz/entity/benzyl-cinnamate-trans (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. 4w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Mass → {'unit': 'Q483261', 'amount': '+238.099'}
    Subclass of → —
    Subclass of → benzyl cinnamate
    Instance of → type of chemical entity
    + 4 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.