ethyl (E/Z)-cinnamate

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q105138131
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ethyl (E/Z)-cinnamate

Summary

ethyl (E/Z)-cinnamate is a group of stereoisomers[1]. It draws 31 Wikipedia views per month (group_of_stereoisomers category, ranking #202 of 1,063).[2]

Key Facts

  • ethyl (E/Z)-cinnamate's instance of is recorded as group of stereoisomers[3].
  • ethyl (E/Z)-cinnamate's CAS Registry Number is recorded as 103-36-6[4].
  • ethyl (E/Z)-cinnamate's canonical SMILES is recorded as O=C(OCC)C=CC=1C=CC=CC1[5].
  • ethyl (E/Z)-cinnamate's InChI is recorded as InChI=1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3[6].
  • ethyl (E/Z)-cinnamate's InChIKey is recorded as KBEBGUQPQBELIU-UHFFFAOYSA-N[7].
  • ethyl (E/Z)-cinnamate's chemical formula is recorded as C₁₁H₁₂O₂[8].
  • ethyl (E/Z)-cinnamate's subclass of is recorded as cinnamate ester[9].
  • ethyl (E/Z)-cinnamate's Commons category is recorded as Ethyl cinnamate[10].
  • ethyl (E/Z)-cinnamate's PubChem CID is recorded as 7649[11].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Origanum syriacum[12].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Mandragora autumnalis[13].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Mandragora officinarum[14].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Artemisia judaica[15].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Cinnamomum zeylanicum[16].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Kaempferia galanga[17].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Narcissus tazetta[18].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Olea europaea[19].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Opuntia ficus-indica[20].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Pandanus tectorius[21].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Swertia japonica[22].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Umbellularia californica[23].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as maize[24].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Hedychium spicatum[25].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Terminalia chebula[26].
  • ethyl (E/Z)-cinnamate's found in taxon is recorded as Ceanothus velutinus[27].

Why It Matters

ethyl (E/Z)-cinnamate draws 31 Wikipedia views per month (group_of_stereoisomers category, ranking #202 of 1,063).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] It is known by 4 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] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . Chemical Composition of Origanum syriacum L. Essential Oil.. wikidata.org.
  11. [13] . Substances isolated from Mandragora species. wikidata.org.
  12. [14] . Substances isolated from Mandragora species. wikidata.org.
  13. [15] . Eudesmanolides from Artemisia judaica. wikidata.org.
  14. [16] . Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils. wikidata.org.
  15. [17] . Studies on crude drugs effective on visceral larva migrans. II. Larvicidal principles in kaempferiae rhizoma. wikidata.org.
  16. [18] . Chemical Investigation and Cytologic Localization of Essential Oils in the Flowers of Narcissus tazetta. wikidata.org.
  17. [19] . Identification of cinnamic acid ethyl ester and 4-vinylphenol in off-flavour olive oils. wikidata.org.
  18. [20] . Volatile constituents of prickly pear (Opuntia ficus indica Mill., de Castilla variety). wikidata.org.
  19. [21] . Isoprene related esters, significant components of Pandanus tectorius. wikidata.org.
  20. [22] . Semburins and Swertiols, Novel 2,8-Dioxabicyclo[3.3.1]nonanes and Their Precursory Alcohols, from Swertia japonica Makino. wikidata.org.
  21. [23] . Terpenoids in Umbellularia californica. wikidata.org.
  22. [24] . Volatile components of corn silk (Zea mays L.): possible Heliothis zea (Boddie) attractants. wikidata.org.
  23. [25] . Phytochemical investigation of labdane diterpenes from the rhizomes of Hedychium spicatum and their cytotoxic activity. wikidata.org.
  24. [26] . Essential oil of Terminalia chebula fruits as a repellent for the indian honeybee Apis florea. wikidata.org.
  25. [27] . An Examination of Ceanothus Velutinus**Scientific Section, A. PH. A., Toronto meeting, 1932.. 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.

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APA 4ort.xyz Knowledge Graph. (2026). ethyl (E/Z)-cinnamate. Retrieved May 3, 2026, from https://4ort.xyz/entity/ethyl-e-z-cinnamate
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BibTeX @misc{4ortxyz_ethyl-e-z-cinnamate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ethyl (E/Z)-cinnamate}}, year = {2026}, url = {https://4ort.xyz/entity/ethyl-e-z-cinnamate}, note = {Accessed: 2026-05-03}}
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