Home › Entities › type_of_chemical_entity › trans-(+)-chrysanthemic acid

trans-(+)-chrysanthemic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q5114537
Press Enter · cited answer in seconds

trans-(+)-chrysanthemic acid

Summary

trans-(+)-chrysanthemic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2]

Key Facts

  • trans-(+)-chrysanthemic acid's instance of is recorded as type of chemical entity[3].
  • trans-(+)-chrysanthemic acid's chemical structure is recorded as Chrysanthemic acid.svg[4].
  • trans-(+)-chrysanthemic acid's CAS Registry Number is recorded as 4638-92-0[5].
  • trans-(+)-chrysanthemic acid's EC number is recorded as 225-067-5[6].
  • trans-(+)-chrysanthemic acid's canonical SMILES is recorded as CC(=CC1C(C1(C)C)C(=O)O)C[7].
  • trans-(+)-chrysanthemic acid's InChI is recorded as InChI=1S/C10H16O2/c1-6(2)5-7-8(9(11)12)10(7,3)4/h5,7-8H,1-4H3,(H,11,12)/t7-,8+/m1/s1[8].
  • trans-(+)-chrysanthemic acid's InChIKey is recorded as XLOPRKKSAJMMEW-SFYZADRCSA-N[9].
  • trans-(+)-chrysanthemic acid's chemical formula is recorded as C₁₀H₁₆O₂[10].
  • trans-(+)-chrysanthemic acid's subclass of is recorded as carboxylic acid[11].
  • trans-(+)-chrysanthemic acid's subclass of is recorded as chrysanthemic acid[12].
  • trans-(+)-chrysanthemic acid's Freebase ID is recorded as /m/0cc6c9g[13].
  • trans-(+)-chrysanthemic acid's UNII is recorded as 23FP207VLY[14].
  • trans-(+)-chrysanthemic acid's ChemSpider ID is recorded as 15876[15].
  • trans-(+)-chrysanthemic acid's PubChem CID is recorded as 16747[16].
  • trans-(+)-chrysanthemic acid's KEGG ID is recorded as C09842[17].
  • trans-(+)-chrysanthemic acid's ChEBI ID is recorded as 39100[18].
  • trans-(+)-chrysanthemic acid's found in taxon is recorded as Tanacetum cinerariifolium[19].
  • trans-(+)-chrysanthemic acid's Reaxys registry number is recorded as 2043419[20].
  • trans-(+)-chrysanthemic acid's Reaxys registry number is recorded as 4904351[21].
  • trans-(+)-chrysanthemic acid's isomeric SMILES is recorded as CC(=C[C@@H]1C@HC(=O)O)CC@HC(=O)O)C">[22].
  • trans-(+)-chrysanthemic acid's LIPID MAPS ID is recorded as LMPR0102060001[23].
  • trans-(+)-chrysanthemic acid's KNApSAcK ID is recorded as C00003031[24].
  • trans-(+)-chrysanthemic acid's mass is recorded as {'unit': 'Q483261', 'amount': '+168.115'}[25].
  • trans-(+)-chrysanthemic acid's Nikkaji ID is recorded as J10.459K[26].
  • trans-(+)-chrysanthemic acid's ECHA Substance Infocard ID is recorded as 100.022.788[27].

Why It Matters

trans-(+)-chrysanthemic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2] It has Wikipedia articles in 7 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] ↑ . 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] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . Production of chrysanthemic acid and pyrethrins by tissue cultures ofChrysanthemum cinerariaefolium. wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEBI. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . ECHA Substance Infocard database. Retrieved . 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-(+)-chrysanthemic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/trans-chrysanthemic-acid
MLA “trans-(+)-chrysanthemic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trans-chrysanthemic-acid.
BibTeX @misc{4ortxyz_trans-chrysanthemic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trans-(+)-chrysanthemic acid}}, year = {2026}, url = {https://4ort.xyz/entity/trans-chrysanthemic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trans-(+)-chrysanthemic acid — https://4ort.xyz/entity/trans-chrysanthemic-acid (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/trans-chrysanthemic-acid · Last refreshed: