Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/709
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dc.contributor.authorSavant, Mahesh M.-
dc.contributor.authorTank, Ravi S.-
dc.contributor.authorKhistariya, Anand V.-
dc.contributor.authorDarshak, Faldu.-
dc.date.accessioned2021-08-19T10:27:28Z-
dc.date.available2021-08-19T10:27:28Z-
dc.date.issued2016-10-01-
dc.identifier.citationSavant, M. M., Tank, R. S., Khistariya, A. V., & Darshak, F. (2016). Synthesis and Characterization of Novel Trisubstituted N-(2-methoxy-4-nitrophenyl)-1-phenyl-5-aryl-1 H-pyrazol-3-Amine Derivatives. Journal of Chemistry and Chemical Sciences, 6(10), 893-901en_US
dc.identifier.issn2229-760X-
dc.identifier.urihttp://www.chemistry-journal.org/detail-chemistry-journal/333/Synthesis-and-Characterization-of-Novel-TrisubstitutedN-methoxy-4-nitrophenyl-phenyl-5-aryl-H-pyrazol-Amine-Derivatives/Mahesh-M-Savant-Ravi-S-Tank-Anand-V-Khistariya-and-Faldu-Darshak.html-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/709-
dc.description.abstractA series of novel trisubstituted pyrazole N-(2-methoxy-4-nitrophenyl)-1- phenyl-5-aryl-1H-pyrazol-3-amine derivatives have been synthesized by the reaction of substituted various novel cinnamamides with phenyl hydrazine. Various cinnamamide were prepared by condensation of appropriate 2-methoxy-4-nitroacetanilide with substituted aldehydes in the presence of sodium hydroxide in ethanol solvent under reflux. We are demonstrating the convenient process for synthesis novel trisubstituted N-(2-methoxy-4-nitrophenyl)-1-phenyl-5-aryl-1H-pyrazol-3-amine derivatives in high yield.en_US
dc.language.isoen_USen_US
dc.publisherJournal of Chemistry and Chemical Sciencesen_US
dc.subjectPyrazole derivatives, 2-methoxy-4-nitroacetanilide, Cinnamamide, Trisubstituted.en_US
dc.titleSynthesis and Characterization of Novel Trisubstituted N-(2-methoxy-4-nitrophenyl)-1-phenyl-5-aryl-1 H-pyrazol-3-Amine Derivativesen_US
dc.typeArticleen_US
Appears in Collections:01. Journal Articles

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