Molecular properties
- Formula
- C15H22O5
- Molar mass
- 282.34 g·mol−1
- Exact mass
- 282.1467 Da
- 5
- PubChem CID
- 68827
Molecule record
(1R,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one
C15H22O5
282.34 g/mol
Loading structure
Functional groups
Alkane / alkyl carbon
Ester
Ether
Physical properties
No source-backed physical properties are curated for this molecule yet.
Common names and synonyms
- (+)-Artemisinin
- (3R,5AS,6R,8AS,9R,12S,12aR)-3,6,9-trimethyloctahydro-3,12-epoxypyrano(4,3-j)-1,2-benzodioxepin-10(3H)-one
- 1,5,9-trimethyl-(1R,4S,5R,9R,12S,13R)-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one
- 2-azanyl-5-methylsulfanyl-pentanoic acid
- 63968-64-9
- 700-290-5
- 9RMU91N5K2
- Arteannuin
Show all 24 synonyms
- Artemisine
- Artemisinina
- Artemisinine
- Artemisininum
- CHEBI:223316
- DTXCID40819890
- DTXSID2040652
- GNF-Pf-5341
- Huanghuahaosu
- NSC-369397
- P01BE01
- Qinghaosu
- RefChem:5566
- artemisinin
- qing hao su
- quinghaosu
Structure identifiers
- Canonical SMILES
- C[C@@H]1CC[C@H]2[C@@H](C)C(=O)O[C@@H]3O[C@@]4(C)CC[C@@H]1[C@]32OO4
- Isomeric SMILES
- C[C@@H]1CC[C@H]2[C@H](C(=O)O[C@H]3[C@@]24[C@H]1CC[C@](O3)(OO4)C)C
- InChI
- InChI=1S/C15H22O5/c1-8-4-5-11-9(2)12(16)17-13-15(11)10(8)6-7-14(3,18-13)19-20-15/h8-11,13H,4-7H2,1-3H3/t8-,9-,10+,11+,13-,14-,15-/m1/s1
- InChIKey
- BLUAFEHZUWYNDE-NNWCWBAJSA-N
- PubChem CID
- 68827
Spectroscopy
Tabs appear only for spectra stored with clear provenance.
No redistributable or simulated spectroscopy record is attached yet.
Simulated NMR
On-demand educational prediction for (1R,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one; not experimental data.
Simulated EI mass spectrum
On-demand educational fragmentation for (1R,4S,5R,8S,9R,12S,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one; not experimental data.
Sources
Molecule identity
Retrieved 8/20/2026. Reuse status is summarized by the badge; open the source for full details.