Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 115-96-8, Name is Tris(2-chloroethyl) phosphate, molecular formula is C6H12Cl3O4P, belongs to thiazolidines compound, is a common compound. In a patnet, author is Abbady, M. A., once mentioned the new application about 115-96-8, Computed Properties of C6H12Cl3O4P.
ORGANIC SELENIUM COMPOUNDS. PART II. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF SOME NEW SYMMETRICAL DIARYLSELENIDES CONTAINING THIAZOLYL, THIAZOLIDIN-4-ONYL, AZETIDIN-2-ONYL, TRIAZOLIN-1-YL AND GLYCYL MOIETIES
4,4-Dimonochloroacetyl diphenylselenide (2) was prepared as a new precursor for the title studies by chloroacetylation of diphenylselenide (1). 2 interacts with thiourea to afford 4,4-di(2-aminothiazol-4-yl)diphenylselenide (3). Condensation of 3 with aromatic aldehydes in the presence of a catalytic amount of dry piperidine furnished aldimines (4). Interaction of 4 with mercaptoacetic acid afforded 4,4-di(2-(2′-substituted phenyl-3′-thiazolo-4′-thiazolidinon)-3′-yl)diphenylselenides (6). Schiff bases 4 interact with mono chloroacetyl chloride in dry dioxane and triethylamine produced 4,4-di(2-(4′-substituted phenyl-3′-chloro-2′-azetidinon-1′-thiazolo)-1′-yl)diphenylselenides (8). 1,3-Dipolar cyclonucleophilic addition of diazomethane to certain of 4 gave 4,4-di(2-(5′-substituted phenyl-(2)-1′,2′,3′-triazoline thiazolo)-1′-yl)diphenylselenides (10). 2 interacts with secondary heteroalicyclic amines to afford 4,4-diglycyl diphenylselenides (11). The structures of the synthesized compounds are based on correct physical data, IR, H-1 NMR, C-13 NMR, and by chemical means. Some of the synthesized compounds were biologically tested.
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Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com