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| 5,7-Dimethoxycoumarin Basic information |
| Product Name: | 5,7-Dimethoxycoumarin | | Synonyms: | 2H-1-Benzopyran-2-one, 5,7-dimethoxy-;5,7-dimethoxy-2h-1-benzopyran-2-on;5,7-Dimethoxy-2H-chromen-2-one;5,7-dimethoxy-1-benzopyran-2-one;NSC 102793;NSC 217987;5,7-dimethoxy-coumari;5,7-dimethyloxy-2H-1-benzopyran-2-one | | CAS: | 487-06-9 | | MF: | C11H10O4 | | MW: | 206.19 | | EINECS: | 207-646-4 | | Product Categories: | Inhibitors;API intermediates;Coumarins | | Mol File: | 487-06-9.mol |
| 5,7-Dimethoxycoumarin Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 43 | | Safety Statements | 36/37 | | WGK Germany | 3 | | RTECS | GN6530000 | | HS Code | 2932209090 |
| 5,7-Dimethoxycoumarin Usage And Synthesis |
| Uses | photosensitizing agent | | Uses | 5,7-Dimethoxycoumarin is a derivitized coumarin compound. | | Synthesis Reference(s) | Journal of the American Chemical Society, 118, p. 6305, 1996 DOI: 10.1021/ja961107i | | General Description | 5,7-dimethoxycoumarin is isolated and identified from leaves and fruits of Pelea anisata H. Mann, a plant whose fruit are used in the construction of mohikana leis. It induces frameshift mutagenesis in bacteria. It also causes lethal photosensitization and the formation of sister chromatid exchanges in Chinese hamster cells. | | Biochem/physiol Actions | 5,7-Dimethoxycoumarin induces the processes of differentiation and melanogenesis in murine (B16) and human (A375). |
| 5,7-Dimethoxycoumarin Preparation Products And Raw materials |
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