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SYNTHESIS AND STUDY OF N,N1 - HEXAMETHYLENE BIS- {[(4,41-DIMETHYLDIPHENYL)-AZO-2,21-DIAMINO] UREA} PROPERTIES, APPLICATIONS

Holboyev Yusufjon KhakimovichDoktor of Philosophy (Ph.D.) of Chemical Sciences, Andijan State Medical Institute, UzbekistanAbdurakhmanov Ulugbek KurganbaevichCandidate of Chemical Sciences, Andijan State Medical Institute, UzbekistanMakhsumov Abdukhamid GafurovichDoctor of Chemical Sciences, professor, Tashkent chemical-technological Institute, UzbekistanValeeva Nailya GennadievnaDoctor of Philosophy (Ph.D.) technical sciences, Tashkent state technical university named after Islam Karimov, Uzbekistan
ABI

Аннотация

The proposed article relates to organic chemical synthesis and the study of bis-azourea compounds, the chemical properties of new N,N1 derivatives - hexamethylene bis-[(4,41-dimethyldiphenyl)-azo-2,21-diamino) ureas]. The interaction of [(4,41-dimethyldiphenyl)-azo-2,21-diamino)-urea] with hexamethylene diisocyanate gave derivatives N,N1 - hexamethylene bis-[(4,41-dimethyldiphenyl)-azo-2,21-diamino) ureas]. The structure of N,N1 - hexamethylene bis-[(4,41-dimethyldiphenyl)-azo-2,21-diamino)urea] was established by elemental analysis, IR and PMR spectroscopy. Reactivity of NH reaction centers N,N1 - hexamethylene bis-[(4,41-dimethyldiphenyl)-azo-2,21-diamino) urea] is studied by the reactions: N,N1-dinitrosation, N,N1-dimetallation, N,N1 -dialkylation, N,N1-dichlorination. Comparative tests show that the tested derivative of the N,N1 compound - hexamethylene bis-[(4,41-dimethyldiphenyl)-azo-2,21-diamino)urea] showed a higher growth-promoting activity.

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