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BioBioPha Co., Ltd.
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0871-65217109 13211707573; |
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| Products Intro: |
Product Name:Spiradine F
CAS:21040-64-2
Purity:95.0% Package:5mg Remarks:BBP00394
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| | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine Basic information |
| Product Name: | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine | | Synonyms: | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine;Spiradine F;12aH,14H-3,14a-Ethano-14,4b,8-ethanylylidene-1H,5H-[2]benzopyrano[4,3-g]oxazolo[3,2-a]azocin-17-ol, decahydro-8-methyl-2-methylene-, 17-acetate, (3S,4aR,4bR,8R,8aS,12aR,14S,14aR,17S,18R)- | | CAS: | 21040-64-2 | | MF: | C24H33NO4 | | MW: | 399.53 | | EINECS: | | | Product Categories: | | | Mol File: | 21040-64-2.mol |  |
| | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine Chemical Properties |
| Boiling point | 510.5±50.0 °C(Predicted) | | density | 1.27±0.1 g/cm3(Predicted) | | pka | 3.79±0.60(Predicted) |
| | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine Usage And Synthesis |
| Description | This alkaloid from Spiraea japonica L. fil. has been obtained as the crystalline
hydrochloride, m.p. l14-7°C. Chemical evidence has shown it to be acetyl_x0002_spiradine G. Oxidation with chromic acid in pyridine yields a hydroxy-Iactam in
which the hydroxyl and lactam groups are formed by oxidative cleavage of an
intermediate alkanolamine ether. | | Uses | Spiradine F is a main alkaloidal component of spiraea japonioa L. fil. Spiradine F derivative can inhibit platelet-activating factor (PAF)-induced platelet aggregation[1][2]. | | References | Toda, Hirata., Tetrahedron Lett., 5565 (1968) |
| | 6β-Acetoxy-15,23-dideoxy-19,23-epoxyajaconine Preparation Products And Raw materials |
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