Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60114
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dc.contributor.authorKrishnan, Radhakrishnan-
dc.contributor.authorPandy, Karthik Manikandan-
dc.contributor.authorParatharaj, Senthil Kumar-
dc.contributor.authorRay, Uttam Kumar-
dc.date.accessioned2022-07-15T11:08:55Z-
dc.date.available2022-07-15T11:08:55Z-
dc.date.issued2022-07-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60114-
dc.description703-716en_US
dc.description.abstractThe new series of N-substituted pyrazoline derivatives bearing benzo[b]thiophene and styryl with trifluoromethyl substitution at para- and meta- positions were synthesized. The structures of newly synthesized compounds were characterized by UV, IR, NMR, Mass and single crystal XRD (SCXRD) and had been screened for antioxidant activity. The in vitro antioxidant activities screening revealed that hydroxyl radical scavenging (HRS) activities of compounds 3c, 3f, 4a, 4e, 4f, 5c, 5d 5e and 5g are stronger than the other compounds and the compound 5g shows much better antioxidant activity.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(07) [July 2022]en_US
dc.subjectPyrazolineen_US
dc.subjectbenzo[b]thiopheneen_US
dc.subjectN-substituted pyrazolinesen_US
dc.subjectantioxidant activityen_US
dc.subjecttrifluoromethyl cinnamaldehydeen_US
dc.titleSynthesis, characterization and antioxidant activities of novel N-substituted pyrazoline derivatives bearing 3-benzo[b]thiophene and 5-styryl substituentsen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(07) [July 2022]

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