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Synthesis & Biological Activity s-Triazine | Synthesis, characterization and in-vitro cytotoxic activity of 2,4,6-trisubstituted-1,3,5-triazine
Language: English
Published by LAP Lambert Academic Publishing, 2012
ISBN 10: 3659104922 ISBN 13: 9783659104923
Taschenbuch. Condition: Neu. Synthesis & Biological Activity s-Triazine | Synthesis, characterization and in-vitro cytotoxic activity of 2,4,6-trisubstituted-1,3,5-triazine | Deepak Kumar Basedia (u. a.) | Taschenbuch | Englisch | LAP Lambert Academic Publishing | EAN 9783659104923 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Synthesis & Biological Activity s-Triazine: Synthesis, characterization and in-vitro cytotoxic activity of 2,4,6-trisubstituted-1,3,5-triazine
Language: English
Published by LAP LAMBERT Academic Publishing, 2012
ISBN 10: 3659104922 ISBN 13: 9783659104923
Paperback. Condition: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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Synthesis & Biological Activity s-Triazine
Language: English
Published by LAP LAMBERT Academic Publishing, 2012
ISBN 10: 3659104922 ISBN 13: 9783659104923
Kartoniert / Broschiert. Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Basedia Deepak KumarDeepak Kumar Basedia is working as Asst. Professor, Department of Pharmaceutical Chemistry, T.I.T. College of Pharmacy, Bhopal (M.P.), India. He has completed his M. Pharm., Pharmaceutical Chemistry from SRM Colle.
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Synthesis & Biological Activity s-Triazine : Synthesis, characterization and in-vitro cytotoxic activity of 2,4,6-trisubstituted-1,3,5-triazine
Language: English
Published by LAP Lambert Academic Publishing, 2012
ISBN 10: 3659104922 ISBN 13: 9783659104923
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Triazine is the chemical species of six-membered heterocyclic ring compound with three nitrogens replacing carbon-hydrogen units in the benzene ring structure. The names of the three isomers indicate which of the carbon-hydrogen units on the benzene ring position of the molecule have been replaced by nitrogens, called 1,2,3-triazine, 1,2,4-triazine, and 1,3,5-triazine respectively. Symmetrical 1,3,5-triazine is the common. Triazines are prepared from cyanic acid amide by trimerization (1,3,5-triazine). Triazines are weak base. Triazines have much weaker resonance energy than benzene, so nucleophilic substitution is preferred than electrophilic substitution. Heterocyclics bearing a symmetrical s-triazines or 1,3,5-triazines moieties, represent an interesting class of compounds possessing a wide spectrum of biological activities such as anti-cancer, antiviral, fungicidal , insecticidal, bactericidal, herbicidal and antimicrobial, antimalarial agents. They also find applications as dyes, lubricants and analytical reagents.
