6028-46-2

Usage

InChI:InChI=1/C12H23O2PS2/c16-15(17,13-11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h11-12H,1-10H2,(H,16,17)

Upstream product

• 108-93-0 cyclohexanol 

Downstream Products

• 7539-17-5 bis(O,O'-di-cyclo-hexylthiophosphoryl)disulphide 
• 26404-46-6 Dithiophosphoric acid S-(1-acetylamino-2,2,2-trichloro-ethyl) ester O,O'-dicyclohexyl ester 
• 135700-26-4 Dithiophosphoric acid O,O'-dicyclohexyl ester; compound with N,N'-diphenyl-guanidine 
• 78923-78-1 C₁₉H₂₇O₃PS₃ 
• 78923-83-8 C₂₀H₂₉O₃PS₃ 
• 91912-65-1 {Pb(C₁₂H₂₂O₂PS₂)2} 

Relevant academic research and scientific papers

Synthesis, spectral characterization and antibacterial activity of O, O’-dialkyl and alkylene dithiophosphatogold (III)dichloride; crystal structure of [S2POCMe2CMe2O]AuCl2

O, O’-Dialkyl and alkylene dithiophosphatogold (III)dichloride complexes of the type [(RO)2PS2]AuCl2 and [S2POGO]AuCl2, where R = Et, nPr, iPr, iBu, Ph, cyclohexyl and cyclopentyl, where G = CMe2CMe2-, have been synthesized in 80-90% yields by reaction of the corresponding acid or sodium salts of the appropriate dithiophosphoric acids in 1:1 ratio with gold (III) chloride in dry dichloromethane at room temperature. The compounds have been characterized by elemental analyses, IR and (1H, l3C, and 31P) NMR. The crystal structure of [S2POCMe2CMe2O]AuCl2, was determined. These new complexes have shown their growth inhibiting potential against various bacterial strains with moderate to good activity.