| Identification | More | [Name]
5,7-Dimethoxycoumarin | [CAS]
487-06-9 | [Synonyms]
5,7-DIMETHOXY-CHROMEN-2-ONE
5,7-DIMETHOXYCOUMARIN
CITROPTEN
CITROPTENE
LIMETIN
LIMETTIN
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-coumari
5,7-dimethyloxy-2H-1-benzopyran-2-one
Citraptene
Coumarin, 5,7-dimethoxy-
5,7-dimethoxy-2-benzopyrone
5,7-Dimethoxycoumarin98%
5,7-DIMETHOXYCOUMARIN WITH HPLC
5,7-Dimethoxycoumarin, Limettin
Citropten, Limettin
5,7-Dimethoxy-2H-1-benzopyran-2-one | [EINECS(EC#)]
207-646-4 | [Molecular Formula]
C11H10O4 | [MDL Number]
MFCD00006870 | [Molecular Weight]
206.19 | [MOL File]
487-06-9.mol |
| Hazard Information | Back Directory | [Uses]
5,7-Dimethoxycoumarin is a derivitized coumarin compound. | [Uses]
photosensitizing agent | [Definition]
ChEBI: 5,7-dimethoxy-1-benzopyran-2-one is a member of coumarins. | [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). | [storage]
Store at -20°C |
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