Catalog Number
ACM58336359-1
Category
Coumarin Dyes; Other Materials
Synonyms
2,3,6,7-Tetrahydro-1H-pyrano[2,3-f]pyrido[3,2,1-ij]quinolin-11(5H)-one
2,3,5,6-1H,4H-Tetrahydroquinolizino[9,9a,1-gh]coumarin
Description
Alfa Chemistry offers high-purity Coumarin 6H products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page.
IUPAC Name
3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,5,7,9(17)-tetraen-4-one
Molecular Formula
C15H15NO2
Canonical SMILES
C1CC2=C3C(=C4C(=C2)C=CC(=O)O4)CCCN3C1
InChI
InChI=1S/C15H15NO2/c17-13-6-5-11-9-10-3-1-7-16-8-2-4-12(14(10)16)15(11)18-13/h5-6,9H,1-4,7-8H2
InChI Key
MZSOXGPKUOAXNY-UHFFFAOYSA-N
Boiling Point
486.3 ± 45.0 °C
Melting Point
128.0 to 132.0 °C
Appearance
Light yellow to Yellow to Orange powder to crystal
Application
Such coumarin dyes are useful for laser dyes emitting blue-green light.
Storage
-20 °C in the dark
Covalently-Bonded Unit Count
1
Exact Mass
241.110279g/mol
Features And Benefits
Coumarins are aromatic lactone compounds, many of which are found in natural plants. Coumarin compounds having an electron donating group at the 7-position show strong light absorption and emission, whereas unsubstituted coumarin compounds hardly emit light. This is because intramolecular charge transfer occurs when both electron-donating and electron-withdrawing groups are present in the coumarin molecule. The introduction of groups at the 3- or 4-position largely controls the wavelength of light absorption and emission. Furthermore, the introduction of electron-withdrawing groups at these positions can enhance the luminescence intensity.
MeSH Entry Terms
coumarin-6H
Monoisotopic Mass
241.110279g/mol
Storage Conditions
Store at room temperature and dry