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5,6-O-benzylidene-L-ascorbic acid

chemical compound
ChemicalSubstance group_of_stereoisomers Q27289686
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5,6-O-benzylidene-L-ascorbic acid

Summary

5,6-O-benzylidene-L-ascorbic acid is a group of stereoisomers[1].

Key Facts

  • 5,6-O-benzylidene-L-ascorbic acid's instance of is recorded as group of stereoisomers[2].
  • 5,6-O-benzylidene-L-ascorbic acid's CAS Registry Number is recorded as 20664-60-2[3].
  • 5,6-O-benzylidene-L-ascorbic acid's canonical SMILES is recorded as C1C(OC(O1)C2=CC=CC=C2)C3C(=C(C(=O)O3)O)O[4].
  • 5,6-O-benzylidene-L-ascorbic acid's InChI is recorded as InChI=1S/C13H12O6/c14-9-10(15)12(16)19-11(9)8-6-17-13(18-8)7-4-2-1-3-5-7/h1-5,8,11,13-15H,6H2/t8-,11+,13?/m0/s1[5].
  • 5,6-O-benzylidene-L-ascorbic acid's InChIKey is recorded as SWTGJCNCBUCXSS-ISUZDFFFSA-N[6].
  • 5,6-O-benzylidene-L-ascorbic acid's chemical formula is recorded as C₁₃H₁₂O₆[7].
  • 5,6-O-benzylidene-L-ascorbic acid's subclass of is recorded as chemical compound[8].
  • 5,6-O-benzylidene-L-ascorbic acid's MeSH descriptor ID is recorded as C070680[9].
  • 5,6-O-benzylidene-L-ascorbic acid's ChEMBL ID is recorded as CHEMBL2221292[10].
  • 5,6-O-benzylidene-L-ascorbic acid's UNII is recorded as T544M6Z94A[11].
  • 5,6-O-benzylidene-L-ascorbic acid's ChemSpider ID is recorded as 16736586[12].
  • 5,6-O-benzylidene-L-ascorbic acid's PubChem CID is recorded as 54682464[13].
  • 5,6-O-benzylidene-L-ascorbic acid's isomeric SMILES is recorded as C1C@H[C@@H]3C(=C(C(=O)O3)O)OC@H[C@@H]3C(=C(C(=O)O3)O)O">[14].
  • 5,6-O-benzylidene-L-ascorbic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+264.063'}[15].
  • 5,6-O-benzylidene-L-ascorbic acid's subject has role is recorded as antineoplastic[16].
  • 5,6-O-benzylidene-L-ascorbic acid's subject has role is recorded as antioxidant[17].
  • 5,6-O-benzylidene-L-ascorbic acid's SureChEMBL ID is recorded as 62540[18].
  • 5,6-O-benzylidene-L-ascorbic acid's DSSTox substance ID is recorded as DTXSID50942865[19].
  • 5,6-O-benzylidene-L-ascorbic acid's DSSTOX compound identifier is recorded as DTXCID201371250[20].
  • 5,6-O-benzylidene-L-ascorbic acid's UniChem compound ID is recorded as 31992660[21].
  • 5,6-O-benzylidene-L-ascorbic acid's Probes And Drugs ID is recorded as PD159771[22].

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] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  9. [10] ↑ . ChEMBL. Retrieved . 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] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  16. [17] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . UniChem. wikidata.org.
  21. [22] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 5,6-O-benzylidene-L-ascorbic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-6-o-benzylidene-l-ascorbic-acid
MLA “5,6-O-benzylidene-L-ascorbic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-6-o-benzylidene-l-ascorbic-acid.
BibTeX @misc{4ortxyz_5-6-o-benzylidene-l-ascorbic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5,6-O-benzylidene-L-ascorbic acid}}, year = {2026}, url = {https://4ort.xyz/entity/5-6-o-benzylidene-l-ascorbic-acid}, note = {Accessed: 2026-05-03}}
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