ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

chemical compound
ChemicalSubstance group_of_stereoisomers Q105302494
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ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

Summary

ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate is a group of stereoisomers[1].

Key Facts

  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's instance of is recorded as group of stereoisomers[2].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's CAS Registry Number is recorded as 102-37-4[3].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's canonical SMILES is recorded as O=C(OCC)C=CC1=CC=C(O)C(O)=C1[4].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's InChI is recorded as InChI=1S/C11H12O4/c1-2-15-11(14)6-4-8-3-5-9(12)10(13)7-8/h3-7,12-13H,2H2,1H3[5].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's InChIKey is recorded as WDKYDMULARNCIS-UHFFFAOYSA-N[6].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's chemical formula is recorded as C₁₁H₁₂O₄[7].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's subclass of is recorded as alkyl caffeate ester[8].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's PubChem CID is recorded as 66883[9].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Aconitum kongboense[10].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Adenocaulon himalaicum[11].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Atractylodes macrocephala[12].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Cichorium glandulosum[13].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Dysoxylum densiflorum[14].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Helichrysum arenarium[15].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Incarvillea delavayi[16].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Incarvillea mairei[17].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Incarvillea mairei var. grandiflora[18].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Isodon eriocalyx[19].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Lespedeza bicolor[20].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Ligularia nelumbifolia[21].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Ligularia veitchiana[22].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Ipomoea nil[23].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Plantago major[24].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Saussurea laniceps[25].
  • ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate's found in taxon is recorded as Smilax china[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . Chemical constituents of the aerial parts of Aconitum kongboense. wikidata.org.
  10. [11] . Phenolic compounds of Aruncus dioicus and Adenocaulon adhaerescens. wikidata.org.
  11. [12] . Chemical constituents of the aerial part of Atractylodes macrocephala. wikidata.org.
  12. [13] . Components of Cichorium glandulosum seeds. wikidata.org.
  13. [14] . Terpenoids from Dysoxylum densiflorum. wikidata.org.
  14. [15] . New flavanone and other constituents of Helichrysum arenarium indigenous to China. wikidata.org.
  15. [16] . Chemical constituents from Incarvillea delavayi. wikidata.org.
  16. [17] . Chemical constituents of Incarvillea mairei var. grandiflora. wikidata.org.
  17. [18] . Chemical constituents of Incarvillea mairei var. grandiflora. wikidata.org.
  18. [19] . Diterpenoids from isodon eriocalyx. wikidata.org.
  19. [20] . New prenylated isoflavanones and other constituents of Lespedeza bicolor. wikidata.org.
  20. [21] . Sinapyl alcohol derivatives and other constituents from Ligularia nelumbifolia. wikidata.org.
  21. [22] . Eremophilanolides from the roots of Ligularia veitchiana. wikidata.org.
  22. [23] . Bioactive Phenolic Constituents from the Seeds of Pharbitis nil. wikidata.org.
  23. [24] . Contents from Plantago major. wikidata.org.
  24. [25] . Two New Lignan Glycosides fromSaussurea laniceps. wikidata.org.
  25. [26] . Steroidal saponins from Smilax china and their anti-inflammatory activities. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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