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3,7-dimethylocta-2,6-dienoic acid

pair of isomeric chemical compounds
ChemicalSubstance group_of_stereoisomers Q61738906
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3,7-dimethylocta-2,6-dienoic acid

Summary

3,7-dimethylocta-2,6-dienoic acid is a group of stereoisomers[1].

Key Facts

  • 3,7-dimethylocta-2,6-dienoic acid's instance of is recorded as group of stereoisomers[2].
  • 3,7-dimethylocta-2,6-dienoic acid's CAS Registry Number is recorded as 459-80-3[3].
  • 3,7-dimethylocta-2,6-dienoic acid's EC number is recorded as 207-299-9[4].
  • 3,7-dimethylocta-2,6-dienoic acid's canonical SMILES is recorded as O=C(O)C=C(C)CCC=C(C)C[5].
  • 3,7-dimethylocta-2,6-dienoic acid's InChI is recorded as InChI=1S/C10H16O2/c1-8(2)5-4-6-9(3)7-10(11)12/h5,7H,4,6H2,1-3H3,(H,11,12)[6].
  • 3,7-dimethylocta-2,6-dienoic acid's InChIKey is recorded as ZHYZQXUYZJNEHD-UHFFFAOYSA-N[7].
  • 3,7-dimethylocta-2,6-dienoic acid's chemical formula is recorded as C₁₀H₁₆O₂[8].
  • 3,7-dimethylocta-2,6-dienoic acid's subclass of is recorded as alpha,beta-unsaturated monocarboxylic acid[9].
  • 3,7-dimethylocta-2,6-dienoic acid's subclass of is recorded as polyunsaturated fatty acid[10].
  • 3,7-dimethylocta-2,6-dienoic acid's subclass of is recorded as methyl-branched fatty acid[11].
  • 3,7-dimethylocta-2,6-dienoic acid's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[12].
  • 3,7-dimethylocta-2,6-dienoic acid's PubChem CID is recorded as 9989[13].
  • 3,7-dimethylocta-2,6-dienoic acid's found in taxon is recorded as Cymbopogon citratus[14].
  • 3,7-dimethylocta-2,6-dienoic acid's found in taxon is recorded as Monocyclanthus vignei[15].
  • 3,7-dimethylocta-2,6-dienoic acid's Human Metabolome Database ID is recorded as HMDB0036103[16].
  • 3,7-dimethylocta-2,6-dienoic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+168.115029752'}[17].
  • 3,7-dimethylocta-2,6-dienoic acid's ECHA Substance Infocard ID is recorded as 100.006.637[18].
  • 3,7-dimethylocta-2,6-dienoic acid's NSC number is recorded as 229335[19].
  • 3,7-dimethylocta-2,6-dienoic acid's SureChEMBL ID is recorded as 794673[20].
  • 3,7-dimethylocta-2,6-dienoic acid's CosIng number is recorded as 40019[21].
  • 3,7-dimethylocta-2,6-dienoic acid's DSSTox substance ID is recorded as DTXSID0047115[22].
  • 3,7-dimethylocta-2,6-dienoic acid's UM-BBD compound ID is recorded as c1045[23].
  • 3,7-dimethylocta-2,6-dienoic acid's DSSTOX compound identifier is recorded as DTXCID8027115[24].
  • 3,7-dimethylocta-2,6-dienoic acid's FL number is recorded as 08.081[25].
  • 3,7-dimethylocta-2,6-dienoic acid's JECFA number is recorded as 1825[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . Identification of geranic acid, a tyrosinase inhibitor in lemongrass (Cymbopogon citratus).. wikidata.org.
  14. [15] ↑ . Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei. wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . CosIng database. Retrieved . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . EFSA database. Retrieved . wikidata.org.
  25. [26] ↑ . Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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