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cis-vanillin 2,3-butanediol acetal

chemical compound
ChemicalSubstance group_of_stereoisomers Q27288767
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Summary

cis-vanillin 2,3-butanediol acetal is a group of stereoisomers[1].

Key Facts

  • cis-vanillin 2,3-butanediol acetal's instance of is recorded as group of stereoisomers[2].
  • cis-vanillin 2,3-butanediol acetal's CAS Registry Number is recorded as 316811-68-4[3].
  • cis-vanillin 2,3-butanediol acetal's canonical SMILES is recorded as CC1C(OC(O1)C2=CC(=C(C=C2)O)OC)C[4].
  • cis-vanillin 2,3-butanediol acetal's InChI is recorded as InChI=1S/C12H16O4/c1-7-8(2)16-12(15-7)9-4-5-10(13)11(6-9)14-3/h4-8,12-13H,1-3H3/t7-,8+,12?[5].
  • cis-vanillin 2,3-butanediol acetal's InChIKey is recorded as JZJHVHUFPUYAJF-ITGSWZIZSA-N[6].
  • cis-vanillin 2,3-butanediol acetal's chemical formula is recorded as C₁₂H₁₆O₄[7].
  • cis-vanillin 2,3-butanediol acetal's subclass of is recorded as chemical compound[8].
  • cis-vanillin 2,3-butanediol acetal's UNII is recorded as S78Z7NJ6E3[9].
  • cis-vanillin 2,3-butanediol acetal's ChemSpider ID is recorded as 32701006[10].
  • cis-vanillin 2,3-butanediol acetal's PubChem CID is recorded as 71587693[11].
  • cis-vanillin 2,3-butanediol acetal's isomeric SMILES is recorded as C[C@@H]1C@@HCC@@HC">[12].
  • cis-vanillin 2,3-butanediol acetal's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+224.105'}[13].
  • cis-vanillin 2,3-butanediol acetal's DSSTox substance ID is recorded as DTXSID00185568[14].
  • cis-vanillin 2,3-butanediol acetal's RxNorm CUI is recorded as 1371314[15].
  • cis-vanillin 2,3-butanediol acetal's DSSTOX compound identifier is recorded as DTXCID40108059[16].
  • cis-vanillin 2,3-butanediol acetal's UniChem compound ID is recorded as 58579158[17].

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 . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  9. [10] ↑ . ChemSpider. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  14. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). cis-vanillin 2,3-butanediol acetal. Retrieved May 3, 2026, from https://4ort.xyz/entity/cis-vanillin-2-3-butanediol-acetal
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BibTeX @misc{4ortxyz_cis-vanillin-2-3-butanediol-acetal_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cis-vanillin 2,3-butanediol acetal}}, year = {2026}, url = {https://4ort.xyz/entity/cis-vanillin-2-3-butanediol-acetal}, note = {Accessed: 2026-05-03}}
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