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| | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl- Basic information |
| Product Name: | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl- | | Synonyms: | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl-;3,4-Dihydro-2-methyl-6-methoxy-7-hydroxyisoquinoline-1(2H)-one;3,4-Dihydro-7-hydroxy-6-methoxy-2-methyl-1(2H)-isoquinolinone;Thalifolin;7-Hydroxy-6-methoxy-2-methyl-3,4-dihydroisoquinolin-1(2H)-one;Thalifoline | | CAS: | 21796-15-6 | | MF: | C11H13NO3 | | MW: | 207.23 | | EINECS: | | | Product Categories: | | | Mol File: | 21796-15-6.mol |  |
| | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl- Chemical Properties |
| Melting point | 210-1°C | | Boiling point | 432.1±45.0 °C(Predicted) | | density | 1.246±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 9.73±0.20(Predicted) | | color | Light yellow to yellow |
| | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl- Usage And Synthesis |
| Description | A simple isoquinoline base, thalifoline occurs in Thalictrum minus and is
obtained in the form of colourless rods when recrystallized from MeOH. The
ultraviolet spectrum in EtOH has absorption maxima at 223.5, 261 and 302 nm.
The structure given has been confirmed by synthesis. | | Uses | Thalifoline is an alkaloid and displays antifungal activity[2]. | | Definition | ChEBI: A natural product found in Arcangelisia gusanlung. | | target | Antifection | | References | Doskotch, Schiff, Beal, Tetrahedron, 25, 469 (1969) |
| | 1(2H)-Isoquinolinone, 3,4-dihydro-7-hydroxy-6-methoxy-2-methyl- Preparation Products And Raw materials |
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