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trans-benzylideneacetone

chemical compound
ChemicalSubstance type_of_chemical_entity Q4380955
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trans-benzylideneacetone

Summary

trans-benzylideneacetone is a type of chemical entity[1]. trans-benzylideneacetone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • trans-benzylideneacetone's instance of is recorded as type of chemical entity[3].
  • trans-benzylideneacetone's chemical structure is recorded as Benzylideneacetone-2D-skeletal.png[4].
  • trans-benzylideneacetone's CAS Registry Number is recorded as 1896-62-4[5].
  • trans-benzylideneacetone's EC number is recorded as 217-587-6[6].
  • trans-benzylideneacetone's canonical SMILES is recorded as CC(=O)C=CC1=CC=CC=C1[7].
  • trans-benzylideneacetone's InChI is recorded as InChI=1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+[8].
  • trans-benzylideneacetone's InChIKey is recorded as BWHOZHOGCMHOBV-BQYQJAHWSA-N[9].
  • trans-benzylideneacetone's chemical formula is recorded as C₁₀H₁₀O[10].
  • trans-benzylideneacetone's subclass of is recorded as benzylideneacetone[11].
  • trans-benzylideneacetone's Commons category is recorded as Benzylideneacetone[12].
  • trans-benzylideneacetone's ChEMBL ID is recorded as CHEMBL73639[13].
  • trans-benzylideneacetone's Freebase ID is recorded as /m/0265_31[14].
  • trans-benzylideneacetone's UNII is recorded as B03X40BMT5[15].
  • trans-benzylideneacetone's RTECS number is recorded as EN0330000[16].
  • trans-benzylideneacetone's ChemSpider ID is recorded as 21106584[17].
  • trans-benzylideneacetone's PubChem CID is recorded as 637759[18].
  • trans-benzylideneacetone's ChEBI ID is recorded as 78399[19].
  • trans-benzylideneacetone's found in taxon is recorded as Polygala senega[20].
  • trans-benzylideneacetone's found in taxon is recorded as Basella alba[21].
  • trans-benzylideneacetone's Reaxys registry number is recorded as 742047[22].
  • trans-benzylideneacetone's isomeric SMILES is recorded as CC(=O)/C=C/C1=CC=CC=C1[23].
  • trans-benzylideneacetone's Human Metabolome Database ID is recorded as HMDB0031617[24].
  • trans-benzylideneacetone's mass is recorded as {'unit': 'Q483261', 'amount': '+146.073'}[25].
  • trans-benzylideneacetone's Nikkaji ID is recorded as J5.357K[26].
  • trans-benzylideneacetone's melting point is recorded as {'unit': 'Q25267', 'amount': '+40.0'}[27].

Why It Matters

trans-benzylideneacetone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] trans-benzylideneacetone has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] trans-benzylideneacetone 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] ↑ . ChEBI. 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] ↑ . wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Q2311683. Retrieved . wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [20] ↑ . Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots. wikidata.org.
  19. [21] ↑ . Volatile flavor components of malabar-nightshade (Basella rubra L.). wikidata.org.
  20. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . Jean-Claude Bradley Open Melting Point Dataset. 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). trans-benzylideneacetone. Retrieved May 3, 2026, from https://4ort.xyz/entity/trans-benzylideneacetone
MLA “trans-benzylideneacetone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trans-benzylideneacetone.
BibTeX @misc{4ortxyz_trans-benzylideneacetone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trans-benzylideneacetone}}, year = {2026}, url = {https://4ort.xyz/entity/trans-benzylideneacetone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trans-benzylideneacetone — https://4ort.xyz/entity/trans-benzylideneacetone (retrieved 2026-05-03)

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