Zade, Varsha S. published the artcileSynthesis and characterization of per-acetylated S-maltosyl 2-isothiobiurets and 2,4-isodithiobiurets and their in vitro antimicrobial activity, Synthetic Route of 3696-23-9, the publication is Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (2015), 54B(6), 815-820, database is CAplus.
A series of S-hepta-O-acetyl-maltosyl-1-aryl-5-p-tolyl-2-isothio-biurets, S-hepta-O-acetyl-maltosyl-1-aryl-5-p-chloro-phenyl-2-isothio-biurets and S-hepta-O-acetyl maltosyl-1-aryl-5-p-tolyl-2,4-isodithio-biurets have been synthesized by the interaction of various S-hepta-O-acetyl maltosyl-1-aryl isothiocarbamides with p-tolyl isocyanate, p-chloro-Ph isocyanate and p-tolyl isothiocyanate resp. The required maltosyl arylisothiocarbamides are synthesized by the displacement of anomeric bromide of acetobromomaltose with aryl thiocarbamides. The identities of these newly synthesized thiomaltosides have been established on the basis of chem. transformations and IR, mass, 1H and 13C NMR spectral studies. These compounds have been screened for their antibacterial and antifungal activities against E. coli, S. aureus, Ps. aeruginosa, S. typhi, R. oligosporus and A. niger. These compounds show most promising activity towards these micro-organisms.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry published new progress about 3696-23-9. 3696-23-9 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Thiourea,Amine,Benzene,Amide, name is 1-(4-Chlorophenyl)thiourea, and the molecular formula is C7H4BrClO2, Synthetic Route of 3696-23-9.
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Chlorides – an overview | ScienceDirect Topics