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Coumarin 521T

Catalog Number
ACM114768728-1
Product Name
Coumarin 521T
Structure
CAS
114768-72-8
Category
Coumarin Dyes
Synonyms
10-Acetyl-2,3,6,7-tetrahydro-1,1,7,7-tetramethyl-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one
Description
Alfa Chemistry offers high-purity Coumarin 521T 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
5-acetyl-10,10,16,16-tetramethyl-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,5,7,9(17)-tetraen-4-one
Molecular Weight
339.44
Molecular Formula
C21H25NO3
Canonical SMILES
CC(=O)C1=CC2=CC3=C4C(=C2OC1=O)C(CCN4CCC3(C)C)(C)C
InChI
InChI=1S/C21H25NO3/c1-12(23)14-10-13-11-15-17-16(18(13)25-19(14)24)21(4,5)7-9-22(17)8-6-20(15,2)3/h10-11H,6-9H2,1-5H3
InChI Key
NGTDVJOJDMQAMI-UHFFFAOYSA-N
Melting Point
278 °C
Purity
>98.0%(HPLC)(N)
Solubility
soluble in Ethanol
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
Complexity
648
Composition
(Nitrogen) 3.90 to 4.40 %
Covalently-Bonded Unit Count
1
Exact Mass
339.183444g/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.
Formal Charge
0
Heavy Atom Count
25
Monoisotopic Mass
339.183444g/mol
Rotatable Bond Count
1
Storage Conditions
Store at room temperature and dry
XLogP3
4.5
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