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(E)-stilbene

chemical compound
ChemicalSubstance type_of_chemical_entity Q306338
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(E)-stilbene

Summary

(E)-stilbene is a type of chemical entity[1]. (E)-stilbene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (92 views/month).[2]

Key Facts

  • (E)-stilbene's instance of is recorded as type of chemical entity[3].
  • (E)-stilbene's chemical structure is recorded as Stilbene trans structure.svg[4].
  • (E)-stilbene's CAS Registry Number is recorded as 103-30-0[5].
  • (E)-stilbene's EC number is recorded as 203-098-5[6].
  • (E)-stilbene's canonical SMILES is recorded as C1=CC=C(C=C1)C=CC2=CC=CC=C2[7].
  • (E)-stilbene's InChI is recorded as InChI=1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H/b12-11+[8].
  • (E)-stilbene's InChIKey is recorded as PJANXHGTPQOBST-VAWYXSNFSA-N[9].
  • (E)-stilbene's chemical formula is recorded as C₁₄H₁₂[10].
  • (E)-stilbene's subclass of is recorded as stilbene[11].
  • (E)-stilbene's Commons category is recorded as Stilbene[12].
  • (E)-stilbene's has part is recorded as carbon[13].
  • (E)-stilbene's has part is recorded as hydrogen[14].
  • (E)-stilbene's ChEMBL ID is recorded as CHEMBL113028[15].
  • (E)-stilbene's Freebase ID is recorded as /m/07nq3r[16].
  • (E)-stilbene's UNII is recorded as 3FA7NW80A0[17].
  • (E)-stilbene's ChemSpider ID is recorded as 553649[18].
  • (E)-stilbene's PubChem CID is recorded as 638088[19].
  • (E)-stilbene's ZVG number is recorded as 492643[20].
  • (E)-stilbene's ChEBI ID is recorded as 36007[21].
  • (E)-stilbene's found in taxon is recorded as Alnus sieboldiana[22].
  • (E)-stilbene's found in taxon is recorded as Petiveria alliacea[23].
  • (E)-stilbene's found in taxon is recorded as Pinus taeda[24].
  • (E)-stilbene's found in taxon is recorded as Alnus firma[25].
  • (E)-stilbene's found in taxon is recorded as Paeonia rockii[26].
  • (E)-stilbene's Gmelin number is recorded as 4381[27].

Why It Matters

(E)-stilbene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (92 views/month).[2] (E)-stilbene has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] (E)-stilbene is known by 13 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] ↑ . 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] ↑ . 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] ↑ . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . Chemical Constituents ofAlnus sieboldiana(BETULACEAE) II. The Isolation and Structure of Flavonoids and Stilbenes. wikidata.org.
  21. [23] ↑ . Trithiolaniacin, a novel trithiolan from Petiveria alliacea. wikidata.org.
  22. [24] ↑ . Diterpenes from pinus taeda. wikidata.org.
  23. [25] ↑ . Chemical Constituents ofAlnus firma(BETULACEAE). I. Phenyl Propane Derivatives Isolated fromAlnus firma. wikidata.org.
  24. [26] ↑ . Bioactive components, antioxidant and antimicrobial activities of Paeonia rockii fruit during development. 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.
  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). (E)-stilbene. Retrieved May 3, 2026, from https://4ort.xyz/entity/e-stilbene
MLA “(E)-stilbene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/e-stilbene.
BibTeX @misc{4ortxyz_e-stilbene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(E)-stilbene}}, year = {2026}, url = {https://4ort.xyz/entity/e-stilbene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (E)-stilbene — https://4ort.xyz/entity/e-stilbene (retrieved 2026-05-03)

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