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(2E/Z)-2-methyl-2-butenal

pair of cis–trans isomers
ChemicalSubstance group_of_stereoisomers Q72509084
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Summary

(2E/Z)-2-methyl-2-butenal is a group of stereoisomers[1].

Key Facts

  • (2E/Z)-2-methyl-2-butenal's instance of is recorded as group of stereoisomers[2].
  • (2E/Z)-2-methyl-2-butenal's CAS Registry Number is recorded as 1115-11-3[3].
  • (2E/Z)-2-methyl-2-butenal's canonical SMILES is recorded as O=CC(=CC)C[4].
  • (2E/Z)-2-methyl-2-butenal's InChI is recorded as InChI=1S/C5H8O/c1-3-5(2)4-6/h3-4H,1-2H3[5].
  • (2E/Z)-2-methyl-2-butenal's InChIKey is recorded as ACWQBUSCFPJUPN-UHFFFAOYSA-N[6].
  • (2E/Z)-2-methyl-2-butenal's chemical formula is recorded as C₅H₈O[7].
  • (2E/Z)-2-methyl-2-butenal's subclass of is recorded as alkenal[8].
  • (2E/Z)-2-methyl-2-butenal's subclass of is recorded as biogenic acyclic aldehyde[9].
  • (2E/Z)-2-methyl-2-butenal's ChemSpider ID is recorded as 9912[10].
  • (2E/Z)-2-methyl-2-butenal's PubChem CID is recorded as 10336[11].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Onion[12].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Aesculus hippocastanum[13].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Allium ampeloprasum[14].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Coffea arabica[15].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Angelica gigas[16].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Camellia sinensis[17].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as tomato[18].
  • (2E/Z)-2-methyl-2-butenal's found in taxon is recorded as Chrysopogon zizanioides[19].
  • (2E/Z)-2-methyl-2-butenal's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+84.057514876'}[20].
  • (2E/Z)-2-methyl-2-butenal's Nikkaji ID is recorded as J126.513J[21].
  • (2E/Z)-2-methyl-2-butenal's SureChEMBL ID is recorded as 258721[22].
  • (2E/Z)-2-methyl-2-butenal's DSSTox substance ID is recorded as DTXSID00859414[23].
  • (2E/Z)-2-methyl-2-butenal's J-GLOBAL ID is recorded as 200907041103944277[24].
  • (2E/Z)-2-methyl-2-butenal's FEMA number is recorded as 3407[25].
  • (2E/Z)-2-methyl-2-butenal's UniChem compound ID is recorded as 26116469[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] ↑ . 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] ↑ . Identification of a new volatile compound in onion (Allium cepa) and leek (Allium porum): 3,4-dimethyl-2,5-dioxo-2,5-dihydrothiophene. wikidata.org.
  12. [13] ↑ . Volatiles of Common Horsechestnut (Aesculus hippocastanumL.) (Hippocastanaceae) Blossoms. wikidata.org.
  13. [14] ↑ . Volatile Compounds in Leek and Asafoetida. wikidata.org.
  14. [15] ↑ . New volatile components of roasted coffee. wikidata.org.
  15. [16] ↑ . Volatile organic compounds of Angelica gigas Nakai, Korean medicinal herb. wikidata.org.
  16. [17] ↑ . Metabolite profiling of Camellia sinensis by automated sequential, multidimensional gas chromatography/mass spectrometry reveals strong monsoon effects on tea constituents. wikidata.org.
  17. [18] ↑ . Differentiation of the volatile profile of microbiologically contaminated canned tomatoes by dynamic headspace extraction followed by gas chromatography-mass spectrometry analysis. wikidata.org.
  18. [19] ↑ . Headspace Constituents of Vetiver Oil. wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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