(+)-trans-allethrin

pair of isomers
ChemicalSubstance group_of_stereoisomers Q27118146
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(+)-trans-allethrin

Summary

(+)-trans-allethrin is a group of stereoisomers[1].

Key Facts

  • (+)-trans-allethrin's instance of is recorded as group of stereoisomers[2].
  • (+)-trans-allethrin's canonical SMILES is recorded as CC1=C(C(=O)CC1OC(=O)C2C(C2(C)C)C=C(C)C)CC=C[3].
  • (+)-trans-allethrin's InChI is recorded as InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3/t14-,16?,17+/m1/s1[4].
  • (+)-trans-allethrin's InChIKey is recorded as ZCVAOQKBXKSDMS-AQYZNVCMSA-N[5].
  • (+)-trans-allethrin's chemical formula is recorded as C₁₉H₂₆O₃[6].
  • (+)-trans-allethrin's subclass of is recorded as allethrin[7].
  • (+)-trans-allethrin's UNII is recorded as G79DM7O471[8].
  • (+)-trans-allethrin's ChemSpider ID is recorded as 18923353[9].
  • (+)-trans-allethrin's PubChem CID is recorded as 15558638[10].
  • (+)-trans-allethrin's ChEBI ID is recorded as 39118[11].
  • (+)-trans-allethrin's ChEBI ID is recorded as 143255[12].
  • (+)-trans-allethrin's Reaxys registry number is recorded as 2702992[13].
  • (+)-trans-allethrin's different from is recorded as Bioallethrin[14].
  • (+)-trans-allethrin's isomeric SMILES is recorded as CC1=C(C(=O)CC1OC(=O)[C@@H]2C@HC=C(C)C)CC=CC@HC=C(C)C)CC=C">[15].
  • (+)-trans-allethrin's LIPID MAPS ID is recorded as LMPR0102060007[16].
  • (+)-trans-allethrin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+302.188195'}[17].
  • (+)-trans-allethrin's subject has role is recorded as insecticide[18].
  • (+)-trans-allethrin's SureChEMBL ID is recorded as 411848[19].
  • (+)-trans-allethrin's DSSTox substance ID is recorded as DTXSID00180679[20].
  • (+)-trans-allethrin's RxNorm CUI is recorded as 19338[21].
  • (+)-trans-allethrin's Probes And Drugs ID is recorded as PD060949[22].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . PubChem. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . Q2311683. Retrieved . wikidata.org.
  9. [10] . PubChem. Retrieved . wikidata.org.
  10. [11] . ChEBI. Retrieved . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . ChEBI. Retrieved . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . PubChem. Retrieved . wikidata.org.
  15. [16] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  16. [17] . PubChem. Retrieved . wikidata.org.
  17. [18] . Medical Subject Headings. Retrieved . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . Global Substance Registration System. Retrieved . wikidata.org.
  21. [22] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. 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-allethrin. Retrieved May 3, 2026, from https://4ort.xyz/entity/-trans-allethrin
MLA “(+)-trans-allethrin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-trans-allethrin.
BibTeX @misc{4ortxyz_-trans-allethrin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(+)-trans-allethrin}}, year = {2026}, url = {https://4ort.xyz/entity/-trans-allethrin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (+)-trans-allethrin — https://4ort.xyz/entity/-trans-allethrin (retrieved 2026-05-03)

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