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Assay
97%
form
solid
mp
135-139 °C (lit.)
SMILES string
NC1=Cc2ccccc2OC1=O
InChI
1S/C9H7NO2/c10-7-5-6-3-1-2-4-8(6)12-9(7)11/h1-5H,10H2
InChI key
QWZHDKGQKYEBKK-UHFFFAOYSA-N
Related Categories
Application
3-Aminocoumarin may be employed in the following studies:
- As ligand for the synthesis of Cr(III), Ni(II), and Cu(II) complexes.
- As starting reagent for the synthesis of 1,2,3,4-tetrahydropyrido[2,3-c]coumarins.
- Synthesis of new 3-(heteroaryl)aminocoumarin derivatives, via optimized Buchwald-Hartwig amination reaction.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Fluorescence spectra of 3-aminocoumarin and its acid-base behaviour in the excited singlet state.
Journal of Photochemistry, 34(1), 55-61 (1986)
Biulleten' eksperimental'noi biologii i meditsiny, 112(10), 358-360 (1991-10-01)
The antioxidant capacity of 3-aminocoumarin, 3-oxycoumarin, 3-acetylaminocoumarin, and 3-coumarin carbonic acid has been investigated with chemiluminescence measurement and by the accumulation of TBA-active products. All coumarins were found to be antioxidants, with 3-oxy-, 3-amino- and 3-acetylamino coumarins being capable of
Hydrolysis-free synthesis of 3-aminocoumarins.
Tetrahedron Letters, 48(29), 5077-5080 (2007)
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