Melting point	172-180 ºC
Specific optical rotation	34 º

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Source	SDS/MSDS Samples
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Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Fluorescence spectra of 3-aminocoumarin and its acid-base behaviour in the excited singlet state. Rao RVS, et al. Journal of Photochemistry, 34(1), 55-61 (1986) High-throughput untargeted screening of veterinary drug residues and metabolites in tilapia using high resolution orbitrap mass spectrometry.Wei Jia et al.Analytica chimica acta, 957, 29-39 (2017-01-22) Effect of Pharmacological Inhibition of the Catalytic Activity of Phosphatases of Regenerating Liver in Early T Cell Receptor Signaling Dynamics and IL-2 Production.Oscar Aguilar-Sopeña et al.International journal of molecular sciences, 21(7) (2020-04-09) Synthesis of biologically potent new 3-(heteroaryl) aminocoumarin derivatives via Buchwald-Hartwig C-N coupling.Das AR, et al. Tetrahedron Letters, 51(7), 1099-1102 (2010) Povarov reactions involving 3-aminocoumarins: synthesis of 1,2,3,4-tetrahydropyrido[2,3-c]coumarins and pyrido[2,3-c]coumarins.Amit A Kudale et al.The Journal of organic chemistry, 73(21), 8437-8447 (2008-09-30) [Antiradical activity of 3-substituted coumarins and their effect on iron-dependent chemiluminescence].Iu A Vladimirov et al.Biulleten' eksperimental'noi biologii i meditsiny, 112(10), 358-360 (1991-10-01) Hydrolysis-free synthesis of 3-aminocoumarins. Kudale AA, et al. Tetrahedron Letters, 48(29), 5077-5080 (2007) Development of novel adenosine receptor ligands based on the 3-amidocoumarin scaffold.Maria J Matos et al.Bioorganic chemistry, 61, 1-6 (2015-06-05) Antimicrobial and antioxidant activities of new metal complexes derived from 3-aminocoumarin.Abdul Amir H Kadhum et al.Molecules (Basel, Switzerland), 16(8), 6969-6984 (2011-08-17)

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