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| | 1-(2,5-Dihydroxy-4-methoxyphenyl)ethanone Basic information |
| | 1-(2,5-Dihydroxy-4-methoxyphenyl)ethanone Chemical Properties |
| | 1-(2,5-Dihydroxy-4-methoxyphenyl)ethanone Usage And Synthesis |
| Uses | 2,5-Dihydroxy-4-methoxyacetophenone (compounds 3) can be isolated from the 80% methanol extract of roots of Cynanchum paniculatum Kitagawa. 2,5-Dihydroxy-4-methoxyacetophenone inhibits glutamate-induced cytotoxicity in hippocampal HT22 cell line[1]. | | Preparation | Preparation by Fries rearrangement of 2-methoxyhydroquinone diacetate, with boron trifluoride in acetic acid (97%); with aluminium chloride in nitrobenzene at r.t., (38%). | | References | [1] Jin Bae Weon, et al. Neuroprotective compounds isolated from Cynanchum paniculatum. Arch Pharm Res. 2012, 35, 4. DOI:10.1007/s12272-012-0404-4 |
| | 1-(2,5-Dihydroxy-4-methoxyphenyl)ethanone Preparation Products And Raw materials |
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