|
| 6,7,8-TRIMETHOXYCOUMARIN Basic information |
Product Name: | 6,7,8-TRIMETHOXYCOUMARIN | Synonyms: | O,O-DIMETHYLFRAXETIN;6,7,8-TRIMETHOXYCOUMARIN;DIMETHYLFRAXETIN, O,O-(RG);DIMETHYLFRAXETIN;DIMETHYLFRAXETIN, O,O-;6,7,8-Trimethoxy-2H-1-benzopyran-2-one;Di-O-Methylfraxetin;Fraxetin dimethyl ether | CAS: | 6035-49-0 | MF: | C12H12O5 | MW: | 236.22 | EINECS: | 200-485-9 | Product Categories: | Coumarins;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract | Mol File: | 6035-49-0.mol | |
| 6,7,8-TRIMETHOXYCOUMARIN Chemical Properties |
Melting point | 104-105°C | Boiling point | 338.68°C (rough estimate) | density | 1.249 | refractive index | 1.5140 (estimate) | storage temp. | 2-8°C | solubility | DMSO : 125 mg/mL (529.17 mM; Need ultrasonic and warming) | form | Cryst. |
Risk Statements | 22 | Safety Statements | 22-45 | HS Code | 29322090 |
| 6,7,8-TRIMETHOXYCOUMARIN Usage And Synthesis |
Chemical Properties | White crystals, soluble in methanol, ethanol, DMSO and other organic solvents, derived from Fraxinuschinensis Roxb. | Uses | Dimethylfraxetin has a bactericidal, anti-inflammatory, anti-radiation damage, and immune-enhancing effects. | Definition | ChEBI: 6,7,8-trimethoxy-1-benzopyran-2-one is a member of coumarins. | Biological Activity | Dimethylfraxetin is a Carbonic anhydrase inhibitor with a Ki of 0.0097 μM. | in vitro | At CA I there is one stand out compound being Dimethylfraxetin (compound 17), a nanomolar CA I inhibitor. This trimethoxy coumarin is the most potent of any of the NP coumarins across the six CA isozymes of the present study . | target | Ki: 0.0097 μM (Carbonic anhydrase) |
| 6,7,8-TRIMETHOXYCOUMARIN Preparation Products And Raw materials |
|