Please use this identifier to cite or link to this item: http://148.72.244.84/xmlui/handle/xmlui/6765
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dc.contributor.authorHussein-R-hammod* Khaled matne - M- * Wassan –B- Ali**-
dc.date.accessioned2023-10-23T19:13:39Z-
dc.date.available2023-10-23T19:13:39Z-
dc.date.issued2016-
dc.identifier.issn2222-8373-
dc.identifier.urihttp://148.72.244.84:8080/xmlui/handle/xmlui/6765-
dc.description.abstractIn this work , new of 5-amino-1,3,4-thiadiazole- 2-thiol derivatives were synthesized (S1- S19), through the reaction of 5-amino-1,3,4-thiadiazole- 2-thiol with p-hydroxy acetophenone to form azo dyes (S2), Chalcones were synthesized by reaction of compound (S2) with different aromatic aldehyde(S3-S6). Compounds (S7-S17) were finally synthesized by ring closure by hydrazine and some hydrazine derivatives . The newly synthesized compounds were confirmed by FT-IR-spectra and H1-NMR, and they showed good agreement with the proposed structures. Also the biological activity of some of the test compounds were investigated in vitro, against some bacterial.en_US
dc.description.sponsorshiphttps://djps.uodiyala.edu.iq/en_US
dc.language.isoenen_US
dc.publisherUniversity of Diyalaen_US
dc.subjectKey words: 5-amino-1,3,4-thiadiazole- 2-thiol , azo dyes , chalcones , ring quinary chalcones.en_US
dc.titleSynthesis and Biological Activity Evolution of 5-amino-1,3,4-thiadiazole- 2- thiol Compound and Some Derivativesen_US
dc.typeArticleen_US
Appears in Collections:مجلة ديالى للعلوم الاكاديمية / Academic Science Journal (Acad. Sci. J.)

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