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14-methyl-hexadeca-8-en-1-ol

group of stereoisomers with the chemical formula C₁₇H₃₄O
ChemicalSubstance group_of_stereoisomers Q110077200
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Summary

14-methyl-hexadeca-8-en-1-ol is a group of stereoisomers[1].

Key Facts

  • 14-methyl-hexadeca-8-en-1-ol's instance of is recorded as group of stereoisomers[2].
  • 14-methyl-hexadeca-8-en-1-ol's canonical SMILES is recorded as OCCCCCCCC=CCCCCC(C)CC[3].
  • 14-methyl-hexadeca-8-en-1-ol's InChI is recorded as InChI=1S/C17H34O/c1-3-17(2)15-13-11-9-7-5-4-6-8-10-12-14-16-18/h5,7,17-18H,3-4,6,8-16H2,1-2H3/b7-5+[4].
  • 14-methyl-hexadeca-8-en-1-ol's InChIKey is recorded as QRFJDYPDABYWFH-FNORWQNLSA-N[5].
  • 14-methyl-hexadeca-8-en-1-ol's chemical formula is recorded as C₁₇H₃₄O[6].
  • 14-methyl-hexadeca-8-en-1-ol's subclass of is recorded as chemical compound[7].
  • 14-methyl-hexadeca-8-en-1-ol's PubChem CID is recorded as 5283286[8].
  • 14-methyl-hexadeca-8-en-1-ol's ChEBI ID is recorded as 188047[9].
  • 14-methyl-hexadeca-8-en-1-ol's found in taxon is recorded as Averrhoa bilimbi[10].
  • 14-methyl-hexadeca-8-en-1-ol's isomeric SMILES is recorded as CCC(C)CCCC/C=C/CCCCCCCO[11].
  • 14-methyl-hexadeca-8-en-1-ol's LIPID MAPS ID is recorded as LMFA05000034[12].
  • 14-methyl-hexadeca-8-en-1-ol's KNApSAcK ID is recorded as C00052558[13].
  • 14-methyl-hexadeca-8-en-1-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+254.260965708'}[14].
  • 14-methyl-hexadeca-8-en-1-ol's SureChEMBL ID is recorded as 832968[15].
  • 14-methyl-hexadeca-8-en-1-ol's UniChem compound ID is recorded as 43631713[16].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2022-06-13. wikidata.org.
  9. [10] ↑ . Antiradical and Xanthine Oxidase Inhibitory Activity Evaluations of L. Leaves and Tentative Identification of Bioactive Constituents through LC-QTOF-MS/MS and Molecular Docking Approach. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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