2-phenylpropanal

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27270639
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2-phenylpropanal

Summary

2-phenylpropanal is a group of stereoisomers[1].

Key Facts

  • 2-phenylpropanal's instance of is recorded as group of stereoisomers[2].
  • 2-phenylpropanal's CAS Registry Number is recorded as 93-53-8[3].
  • 2-phenylpropanal's EC number is recorded as 202-255-5[4].
  • 2-phenylpropanal's canonical SMILES is recorded as CC(C=O)C1=CC=CC=C1[5].
  • 2-phenylpropanal's InChI is recorded as InChI=1S/C9H10O/c1-8(7-10)9-5-3-2-4-6-9/h2-8H,1H3[6].
  • 2-phenylpropanal's InChIKey is recorded as IQVAERDLDAZARL-UHFFFAOYSA-N[7].
  • 2-phenylpropanal's chemical formula is recorded as C₉H₁₀O[8].
  • 2-phenylpropanal's subclass of is recorded as phenyl compound[9].
  • 2-phenylpropanal's subclass of is recorded as aldehydes[10].
  • 2-phenylpropanal's UNII is recorded as 8JKX55PKZQ[11].
  • 2-phenylpropanal's ChemSpider ID is recorded as 6879[12].
  • 2-phenylpropanal's PubChem CID is recorded as 7146[13].
  • 2-phenylpropanal's ZVG number is recorded as 492538[14].
  • 2-phenylpropanal's ChEBI ID is recorded as 149463[15].
  • 2-phenylpropanal's found in taxon is recorded as Vitex agnus-castus[16].
  • 2-phenylpropanal's found in taxon is recorded as Gossypium hirsutum[17].
  • 2-phenylpropanal's found in taxon is recorded as Swertia japonica[18].
  • 2-phenylpropanal's Human Metabolome Database ID is recorded as HMDB0031626[19].
  • 2-phenylpropanal's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+134.073'}[20].
  • 2-phenylpropanal's ECHA Substance Infocard ID is recorded as 100.002.051[21].
  • 2-phenylpropanal's Google Knowledge Graph ID is recorded as /g/11fzyrh0__[22].
  • 2-phenylpropanal's NSC number is recorded as 5231[23].
  • 2-phenylpropanal's SureChEMBL ID is recorded as 60688[24].
  • 2-phenylpropanal's CosIng number is recorded as 40264[25].
  • 2-phenylpropanal's DSSTox substance ID is recorded as DTXSID0052629[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] . Global Substance Registration System. Retrieved . wikidata.org.
  11. [12] . Q2311683. Retrieved . wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . ChEBI release 2021-03-01. wikidata.org.
  15. [16] . Essential Oil Composition of Leaves and Berries ofVitex agnus-castusL. from Calabria, Southern Italy. wikidata.org.
  16. [17] . Survey of the volatile constituents of cotton lint and waste with regard to byssinosis. wikidata.org.
  17. [18] . Semburins and Swertiols, Novel 2,8-Dioxabicyclo[3.3.1]nonanes and Their Precursory Alcohols, from Swertia japonica Makino. wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . PubChem. Retrieved . wikidata.org.
  20. [21] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  21. [22] . 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). 2-phenylpropanal. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-phenylpropanal
MLA “2-phenylpropanal.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-phenylpropanal.
BibTeX @misc{4ortxyz_2-phenylpropanal_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-phenylpropanal}}, year = {2026}, url = {https://4ort.xyz/entity/2-phenylpropanal}, note = {Accessed: 2026-05-03}}
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