Introduction：Basic information about 2,3-DIHYDROXY-4-METHOXYACETOPHENONE CAS 708-53-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
2,3-DIHYDROXY-4-METHOXYACETOPHENONE Basic information
| Product Name: | 2,3-DIHYDROXY-4-METHOXYACETOPHENONE |
| Synonyms: | 1-(2,3-DIHYDROXY-4-METHOXYPHENYL)ETHANONE;Gallacetophenone 4-O-methyl ether;NSC 46636;GALLACETOPHENONE-4'-METHYL ETHER;GALLACETOPHENONE-4-METHYL ETHER;4-METHOXY-2,3-DIHYDROXYACETOPHENONE;2',3'-DIHYDROXY-4'-METHOXYACETOHPENONE, HYDRATE;2,3-DIHYDROXY-4-METHOXYACETOPHENONE |
| CAS: | 708-53-2 |
| MF: | C9H10O4 |
| MW: | 182.17 |
| EINECS: | |
| Product Categories: | Aromatic Acetophenones & Derivatives (substituted) |
| Mol File: | 708-53-2.mol |
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2,3-DIHYDROXY-4-METHOXYACETOPHENONE Chemical Properties
| Melting point | 133 °C |
| Boiling point | 359.6±42.0 °C(Predicted) |
| density | 1.284±0.06 g/cm3(Predicted) |
| storage temp. | Inert atmosphere,Room Temperature |
| form | powder to crystal |
| pka | 8.98±0.15(Predicted) |
| color | Light yellow to Yellow to Green |
Safety Information
2,3-DIHYDROXY-4-METHOXYACETOPHENONE Usage And Synthesis
| Uses | 1-(2,3-Dihydroxy-4-methoxyphenyl)ethanone is a a neuroprotective compound isolated from Cynenchum paniculatum. It exerts neuroprotective and cognitive-enhancing activities through its antioxidant activity and may be helpful for the treatment of Alzheimer''s disease. |
| Preparation | Preparation by reaction of acetic acid on pyrogallol 1-methyl ether, ? with zinc chloride at reflux (155–160°) (Nencki reaction); ? with boron trifluoride on a steam bath (77%). |
| in vivo | 2,3-dihydroxy-4-methoxyacetophenone (50mg/kg; po) improves the impairment of spatial memory induced by scopolamine[1]. |
2,3-DIHYDROXY-4-METHOXYACETOPHENONE Preparation Products And Raw materials
