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| | aucubigenin Basic information |
| Product Name: | aucubigenin | | Synonyms: | aucubigenin;(1R)-1,4aα,5,7aα-Tetrahydro-7-(hydroxymethyl)cyclopenta[c]pyran-1α,5α-diol;Cyclopenta[c]pyran-1,5-diol, 1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-, (1R,4aR,5S,7aS)-;(1R,4aR,5S,7aS)-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1,5-diol | | CAS: | 64274-28-8 | | MF: | C9H12O4 | | MW: | 184.19 | | EINECS: | | | Product Categories: | | | Mol File: | 64274-28-8.mol |  |
| | aucubigenin Chemical Properties |
| Melting point | 110-111 °C(Solv: ethyl acetate (141-78-6)) | | Boiling point | 442.7±45.0 °C(Predicted) | | density | 1.429±0.06 g/cm3(Predicted) | | pka | 12.23±0.60(Predicted) |
| | aucubigenin Usage And Synthesis |
| Uses | Aucubigenin, the aglycone of the iridoid glycoside aucubin, has been characterized through X-ray diffraction analysis. Its crystal structure reveals monoclinic symmetry with specific conformations adopted by its cyclopentane and pyran rings. The study also determined the absolute configurations of both aucubin and aucubigenin. Significant O-H O hydrogen bonding interactions were observed in the crystal lattices of both compounds, highlighting their structural stability and potential for intermolecular interactions[1]. | | References | [1] X-ray crystal structure of iridoid glucoside aucubin and its aglycone |
| | aucubigenin Preparation Products And Raw materials |
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