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(2E)-citronellyl 2-methylbut-2-enoate

chemical compound
ChemicalSubstance group_of_stereoisomers Q27292256
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Summary

(2E)-citronellyl 2-methylbut-2-enoate is a group of stereoisomers[1].

Key Facts

  • (2E)-citronellyl 2-methylbut-2-enoate's instance of is recorded as group of stereoisomers[2].
  • (2E)-citronellyl 2-methylbut-2-enoate's CAS Registry Number is recorded as 24717-85-9[3].
  • (2E)-citronellyl 2-methylbut-2-enoate's EC number is recorded as 246-426-2[4].
  • (2E)-citronellyl 2-methylbut-2-enoate's canonical SMILES is recorded as CC=C(C)C(=O)OCCC(C)CCC=C(C)C[5].
  • (2E)-citronellyl 2-methylbut-2-enoate's InChI is recorded as InChI=1S/C15H26O2/c1-6-14(5)15(16)17-11-10-13(4)9-7-8-12(2)3/h6,8,13H,7,9-11H2,1-5H3/b14-6+[6].
  • (2E)-citronellyl 2-methylbut-2-enoate's InChIKey is recorded as UCFQYMKLDPWFHZ-MKMNVTDBSA-N[7].
  • (2E)-citronellyl 2-methylbut-2-enoate's chemical formula is recorded as C₁₅H₂₆O₂[8].
  • (2E)-citronellyl 2-methylbut-2-enoate's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[9].
  • (2E)-citronellyl 2-methylbut-2-enoate's subclass of is recorded as biogenic acyclic ester[10].
  • (2E)-citronellyl 2-methylbut-2-enoate's subclass of is recorded as wax monoester[11].
  • (2E)-citronellyl 2-methylbut-2-enoate's UNII is recorded as W3KE673ROS[12].
  • (2E)-citronellyl 2-methylbut-2-enoate's ChemSpider ID is recorded as 4905187[13].
  • (2E)-citronellyl 2-methylbut-2-enoate's ChemSpider ID is recorded as 21427814[14].
  • (2E)-citronellyl 2-methylbut-2-enoate's PubChem CID is recorded as 6386037[15].
  • (2E)-citronellyl 2-methylbut-2-enoate's found in taxon is recorded as Geranium[16].
  • (2E)-citronellyl 2-methylbut-2-enoate's found in taxon is recorded as Pelargonium ternifolium[17].
  • (2E)-citronellyl 2-methylbut-2-enoate's isomeric SMILES is recorded as C/C=C(\C)/C(=O)OCCC(C)CCC=C(C)C[18].
  • (2E)-citronellyl 2-methylbut-2-enoate's Human Metabolome Database ID is recorded as HMDB0032209[19].
  • (2E)-citronellyl 2-methylbut-2-enoate's LIPID MAPS ID is recorded as LMFA07010821[20].
  • (2E)-citronellyl 2-methylbut-2-enoate's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+238.193'}[21].
  • (2E)-citronellyl 2-methylbut-2-enoate's ECHA Substance Infocard ID is recorded as 100.042.191[22].
  • (2E)-citronellyl 2-methylbut-2-enoate's SureChEMBL ID is recorded as 16356747[23].
  • (2E)-citronellyl 2-methylbut-2-enoate's SureChEMBL ID is recorded as 873826[24].
  • (2E)-citronellyl 2-methylbut-2-enoate's CosIng number is recorded as 39559[25].
  • (2E)-citronellyl 2-methylbut-2-enoate's DSSTox substance ID is recorded as DTXSID3051911[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [13] ↑ . ChemSpider. Retrieved . wikidata.org.
  13. [14] ↑ . ChemSpider. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . Chemical and Agronomical Investigations of a New Chemotype of Geranium. wikidata.org.
  16. [17] ↑ . Composition of the Oil of Rose-Scented Geranium (Pelargonium sp.) Grown Under the Semiarid Tropical Climate of South India. wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  20. [21] ↑ . PubChem. Retrieved . wikidata.org.
  21. [22] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . CosIng database. Retrieved . wikidata.org.
  25. [26] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). (2E)-citronellyl 2-methylbut-2-enoate. Retrieved May 3, 2026, from https://4ort.xyz/entity/-2e-citronellyl-2-methylbut-2-enoate
MLA “(2E)-citronellyl 2-methylbut-2-enoate.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-2e-citronellyl-2-methylbut-2-enoate.
BibTeX @misc{4ortxyz_-2e-citronellyl-2-methylbut-2-enoate_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(2E)-citronellyl 2-methylbut-2-enoate}}, year = {2026}, url = {https://4ort.xyz/entity/-2e-citronellyl-2-methylbut-2-enoate}, note = {Accessed: 2026-05-03}}
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