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

Authors

  • Holboyev Yusufjon Khakimovich
  • Abdurakhmanov Ulugbek Kurganbaevich
  • Makhsumov Abdukhamid Gafurovich
  • Valeeva Nailya Gennadievna

DOI:

https://doi.org/10.47750/pnr.2022.13.S06.441

Keywords:

phenyl, azogroups, urea, polyhydrocarbongroups, intensification, fixation, fabrics, natural, chemical fibers, dyes, textile, materials, dinitrosation, demetallation, dialkylation, dichlorination, polymers.

Abstract

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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Published

2022-10-20

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Articles

How to Cite

SYNTHESIS AND STUDY OF N,N1 - HEXAMETHYLENE BIS- {[(4,41-DIMETHYLDIPHENYL)-AZO-2,21-DIAMINO] UREA} PROPERTIES, APPLICATIONS. (2022). Journal of Pharmaceutical Negative Results, 3265-2378. https://doi.org/10.47750/pnr.2022.13.S06.441