New explortion of 14348-75-5

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Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Hamidinasab, Mahdia, once mentioned the application of 14348-75-5, Name is 2,7-Dibromo-9H-fluoren-9-one, molecular formula is C13H6Br2O, molecular weight is 337.99, MDL number is MFCD00010790, category is phthalazines. Now introduce a scientific discovery about this category, Application In Synthesis of 2,7-Dibromo-9H-fluoren-9-one.

Green synthesis of 1H-pyrazolo[1,2-b]phthalazine-2-carbonitrile derivatives using a new bifunctional base-ionic liquid hybrid magnetic nanocatalyst

The ionic liquid-base N,N,2,2,6,6-hexamethyl-N-(3-(trimethoxysilyl)propyl)piperidin-4-amonium iodide was grafted onto titana-coated NiFe2O4 nanoparticles for obtaining an efficient and reusable ionic liquid-base hybrid nanocatalyst. The structure of hybrid nanoparticles was characterized using FT-IR (Fourier-transform infrared spectroscopy), field emission scanning electron microscopy, EDS (energy-dispersive X-ray spectroscopy), EDS map scan, Brunauer-Emmett-Teller surface area analysis, CHN (elemental analysis), vibrating sample magnetometer and thermogravimetric analysis techniques. Furthermore, this novel hybrid catalyst was used in one-pot three-component synthesis of 3-amino-1-aryl-5,10-dioxo-1H-pyrazolo[1,2-b]phthalazine-2-carbonitrile derivatives under green and environmentally benign conditions. This protocol avoids the use of harmful catalysts, toxic solvents and harsh reaction conditions. The products were synthesized in excellent yields within short reaction time and identified using elemental analysis, FT-IR, H-1 NMR and C-13 NMR spectroscopies.

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Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem