| 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 |
| Chemical Properties | Back Directory | [Melting point ]
146-149 °C (lit.) | [Boiling point ]
305.04°C (rough estimate) | [density ]
1.2607 (rough estimate) | [refractive index ]
1.4570 (estimate) | [storage temp. ]
2-8°C
| [solubility ]
Acetonitrile (Slightly), Chloroform (Slightly) | [form ]
Solid | [color ]
White to Off-White | [Merck ]
14,5492 | [Major Application]
food and beverages | [InChI]
1S/C11H10O4/c1-13-7-5-9(14-2)8-3-4-11(12)15-10(8)6-7/h3-6H,1-2H3 | [InChIKey]
NXJCRELRQHZBQA-UHFFFAOYSA-N | [SMILES]
COc1cc(OC)c2C=CC(=O)Oc2c1 | [LogP]
1.891 (est) | [CAS DataBase Reference]
487-06-9(CAS DataBase Reference) | [NIST Chemistry Reference]
2H-1-benzopyran-2-one, 5,7-dimethoxy-(487-06-9) | [EPA Substance Registry System]
487-06-9(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
43 | [Safety Statements ]
36/37 | [WGK Germany ]
3
| [RTECS ]
GN6530000
| [HS Code ]
2932209090 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Buddha's hand. | [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 |
|
| Company Name: |
Alfa Aesar
|
| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|