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Cinncassiol A

chemical compound
ChemicalSubstance group_of_stereoisomers Q27155183
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Cinncassiol A

Summary

Cinncassiol An is a group of stereoisomers[1].

Key Facts

  • Cinncassiol A's instance of is recorded as group of stereoisomers[2].
  • Cinncassiol A's canonical SMILES is recorded as CC1CCC2(C3(CC(=O)OC2(C1O)C4(C3(CC(=C4C)C(C)CO)O)O)C)O[3].
  • Cinncassiol A's InChI is recorded as InChI=1S/C20H30O7/c1-10-5-6-17(24)16(4)8-14(22)27-20(17,15(10)23)19(26)12(3)13(11(2)9-21)7-18(16,19)25/h10-11,15,21,23-26H,5-9H2,1-4H3/t10-,11?,15+,16-,17-,18+,19+,20+/m0/s1[4].
  • Cinncassiol A's InChIKey is recorded as WIFHAKQJYHVTQK-TZKDRYALSA-N[5].
  • Cinncassiol A's chemical formula is recorded as C₂₀H₃₀O₇[6].
  • Cinncassiol A's subclass of is recorded as chemical compound[7].
  • Cinncassiol A's ChemSpider ID is recorded as 30791608[8].
  • Cinncassiol A's PubChem CID is recorded as 46173967[9].
  • Cinncassiol A's KEGG ID is recorded as C17645[10].
  • Cinncassiol A's ChEBI ID is recorded as 81241[11].
  • Cinncassiol A's found in taxon is recorded as Cinnamomum cassia[12].
  • Cinncassiol A's found in taxon is recorded as Cinnamomum burmanni[13].
  • Cinncassiol A's isomeric SMILES is recorded as C[C@H]1CC[C@@]2([C@@]3(CC(=O)O[C@@]2([C@@H]1O)[C@@]4([C@]3(CC(=C4C)C(C)CO)O)O)C)O[14].
  • Cinncassiol A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+382.199153'}[15].
  • Cinncassiol A's SureChEMBL ID is recorded as 29683421[16].
  • Cinncassiol A's UniChem compound ID is recorded as 1070569[17].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Q2311683. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Studies on the constituents of cinnamomi cortex. VI. On the mass spectrometry of cassia diterpene (lactone type) (author's transl). wikidata.org.
  12. [13] ↑ . Studies on the constituents of cinnamomi cortex. VI. On the mass spectrometry of cassia diterpene (lactone type) (author's transl). wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . 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). Cinncassiol A. Retrieved May 3, 2026, from https://4ort.xyz/entity/cinncassiol-a
MLA “Cinncassiol A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cinncassiol-a.
BibTeX @misc{4ortxyz_cinncassiol-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Cinncassiol A}}, year = {2026}, url = {https://4ort.xyz/entity/cinncassiol-a}, note = {Accessed: 2026-05-03}}
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