Melting point	237-240 ºC (分解)**
Density	1.743±0.06 g/cm3 (20 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

Synthesis of quinolines from 3-formylchromone.Andrey S Plaskon et al.The Journal of organic chemistry, 73(15), 6010-6013 (2008-07-03) Loss of H2 and CO from protonated aldehydes in electrospray ionization mass spectrometry.Pedatsur Neta et al.Rapid communications in mass spectrometry : RCM, 28(17), 1871-1882 (2014-08-05) Synthesis and biological evaluation of pyrano[4,3-b][1]benzopyranone derivatives as monoamine oxidase and cholinesterase inhibitors.Koichi Takao et al.Bioorganic chemistry, 83, 432-437 (2018-11-15) Hypoxia efficient and glutathione-resistant cytoselective ruthenium(II)-p-cymene-arylimidazophenanthroline complexes: biomolecular interaction and live cell imaging.Ashaparna Mondal et al.Dalton transactions (Cambridge, England : 2003), 49(36), 12865-12878 (2020-09-11) DNA interaction studies of rhenium compounds with Schiff base chelates encompassing biologically relevant moieties.Muhammed Bilaal Ismail et al.Nucleosides, nucleotides & nucleic acids, 38(12), 950-971 (2019-07-11) Coumarin Derived "Turn on" Fluorescent Sensor for Selective Detection of Cadmium (II) Ion: Spectroscopic Studies and Validation of Sensing Mechanism by DFT Calculations.Siffeen Zehra et al.Journal of fluorescence, 29(4), 1029-1037 (2019-07-22) Formylchromone exhibits salubrious effects against nitrosodiethylamine mediated early hepatocellular carcinogenesis in rats.M Ilamathi et al.Chemico-biological interactions, 219, 175-183 (2014-06-24) A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones.Pitchaimani Prasanna et al.Beilstein journal of organic chemistry, 10, 459-465 (2014-03-13) 3-Formylchromones: potential antiinflammatory agents.Khalid M Khan et al.European journal of medicinal chemistry, 45(9), 4058-4064 (2010-06-26) Thermal solvent-free synthesis of chromonyl chalcones, pyrazolines and their in vitro antibacterial, antifungal activities.Zeba N Siddiqui et al.Journal of enzyme inhibition and medicinal chemistry, 27(1), 84-91 (2011-05-27)

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