di-p-methylbenzylidenesorbitol

chemical compound
ChemicalSubstance group_of_stereoisomers Q27231383
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Summary

di-p-methylbenzylidenesorbitol is a group of stereoisomers[1].

Key Facts

  • di-p-methylbenzylidenesorbitol's instance of is recorded as group of stereoisomers[2].
  • di-p-methylbenzylidenesorbitol's CAS Registry Number is recorded as 81541-12-0[3].
  • di-p-methylbenzylidenesorbitol's EC number is recorded as 617-241-8[4].
  • di-p-methylbenzylidenesorbitol's canonical SMILES is recorded as CC1=CC=C(C=C1)C2OCC3C(O2)C(OC(O3)C4=CC=C(C=C4)C)C(CO)O[5].
  • di-p-methylbenzylidenesorbitol's InChI is recorded as InChI=1S/C22H26O6/c1-13-3-7-15(8-4-13)21-25-12-18-20(28-21)19(17(24)11-23)27-22(26-18)16-9-5-14(2)6-10-16/h3-10,17-24H,11-12H2,1-2H3/t17-,18+,19-,20-,21?,22?/m1/s1[6].
  • di-p-methylbenzylidenesorbitol's InChIKey is recorded as LQAFKEDMOAMGAK-RLCYQCIGSA-N[7].
  • di-p-methylbenzylidenesorbitol's chemical formula is recorded as C₂₂H₂₆O₆[8].
  • di-p-methylbenzylidenesorbitol's subclass of is recorded as chemical compound[9].
  • di-p-methylbenzylidenesorbitol's ChEMBL ID is recorded as CHEMBL3561699[10].
  • di-p-methylbenzylidenesorbitol's UNII is recorded as 00YK2U88F9[11].
  • di-p-methylbenzylidenesorbitol's ChemSpider ID is recorded as 5254121[12].
  • di-p-methylbenzylidenesorbitol's PubChem CID is recorded as 6850837[13].
  • di-p-methylbenzylidenesorbitol's isomeric SMILES is recorded as CC1=CC=C(C=C1)C2OC[C@H]3C@@HC@HC@@HOC@@HC@HC@@HO">[14].
  • di-p-methylbenzylidenesorbitol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+386.173'}[15].
  • di-p-methylbenzylidenesorbitol's ECHA Substance Infocard ID is recorded as 100.115.914[16].
  • di-p-methylbenzylidenesorbitol's SureChEMBL ID is recorded as 1966771[17].
  • di-p-methylbenzylidenesorbitol's DSSTox substance ID is recorded as DTXSID3051381[18].
  • di-p-methylbenzylidenesorbitol's DSSTOX compound identifier is recorded as DTXCID4029983[19].
  • di-p-methylbenzylidenesorbitol's UniChem compound ID is recorded as 23654920[20].

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] ↑ . ECHA Substance Infocard database. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [11] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  11. [12] ↑ . ChemSpider. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). di-p-methylbenzylidenesorbitol. Retrieved May 3, 2026, from https://4ort.xyz/entity/di-p-methylbenzylidenesorbitol
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BibTeX @misc{4ortxyz_di-p-methylbenzylidenesorbitol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{di-p-methylbenzylidenesorbitol}}, year = {2026}, url = {https://4ort.xyz/entity/di-p-methylbenzylidenesorbitol}, note = {Accessed: 2026-05-03}}
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