21 research outputs found

    Efficient Synthesis of 4-Hydroxybenzo[ h

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    Growth, electrical, thermal, mechanical and etching studies on 4-chloroanilinium hydrogen (2R, 3R)-tartrate monohydrate-an organic NLO single crystal

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    An organic single crystal of 4-chloroanilinium hydrogen (2R,3R)-tartrate monohydrate (4CAHT) was grown by slow evaporation solution growth technique at room temperature. Single crystal XRD study confirmed that the crystal belongs to monoclinic system with the space group P21. Powder XRD analysis confirmed the crystalline nature of the compound. The presence of various functional groups in the compound was revealed by FT-IR analysis. UV studies showed the absence of absorption in the entire visible region. To determine the thermal stability of the grown crystals it was subjected to thermogravimetric and differential thermal analyses. Microhardness and etching studies were also carried out for the crystal. The powder second harmonic generation efficiency of 4CAHT was tested by Kurtz and Perry powder technique and the relative SHG efficiency of 4CAHT was found to be 1.44 times greater than that of standard KDP

    Microwave-assisted solvent-free synthesis of 4-methyl-2-hydroxy- and 2-methyl-4-hydroxyquinolines

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    1203-1207Rapid and efficient microwave-assisted synthesis of 4-methyl-2-hydroxy- and 2-methyl-4-hydroxyquinolines from anilines and ethyl acetoacetate under different conditions is described

    An efficient synthesis of 9(10<i style="">H</i>)-acridinones under microwaves

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    1958-1960N-Phenylanthranilic acids have been subjected to cyclisation with different catalysts like silica gel, acidic alumina, strongly acidic montmorillonite (K10) clay, acetic acid, PTSA or Lewis acids like ZnCl2, AlCl3 and PPA under microwave irradiation to give 9(10H)-acridinones of which PPA has been found to be the best catalyst for cyclisation

    One-pot multicomponent synthesis of some novel acridines

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    1703-1706Acridine derivatives 1b-5b have been synthesized from dimedone, 1,3-cyclohexanedione, cyclohexanone and phenols by reacting each with vinyl acetate in 2% sodium hydroxide followed by treatment with ammonia
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