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InChI:InChI=1/C5H11NO2S2/c7-3-1-6(2-4-8)5(9)10/h7-8H,1-4H2,(H,9,10)/p-1

Upstream product

• 111-42-2 2,2'-iminobis[ethanol] 
• 75-15-0 carbon disulfide 

Downstream Products

• 10591-85-2 bis(dibenzylthiocarbamoyl)disulfide 

Relevant academic research and scientific papers

CoFe2O4/CdS nanocomposite: Preparation, characterisation, and application in sonocatalytic degradation of organic dye pollutants

A magnetic CoFe2O4/CdS nanocomposite was prepared via one-step hydrothermal decomposition of cadmium diethanoldithiocarbamate complex on the surface of CoFe2O4 nanoparticles at a low temperature of 200 °C. The nanocomposite was characterised by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDX), UV-visible spectroscopy, transmission electron microscopy (TEM), N2 gas sorption analysis, X-ray photoelectron spectroscopy (XPS), and vibrating sample magnetometry. The FT-IR, XRD, EDX and XPS results confirmed the formation of the CoFe2O4/CdS nanocomposite. Based on the TEM analysis, the CoFe2O4/CdS nanocomposite constituted nearly uniform, sphere-like nanoparticles of ～20 nm in size. The optical absorption spectrum of the CoFe2O4/CdS nanocomposite displayed a band gap of 2.21 eV, which made it a suitable candidate for application in sono/photocatalytic degradation of organic pollutants. Accordingly, the sonocatalytic activity of the CoFe2O4/CdS nanocomposite was evaluated towards the H2O2-assisted degradation of methylene blue, rhodamine B, and methyl orange under ultrasonic irradiation. The nanocomposite displayed excellent sonocatalytic activity towards the degradation of all dyes examined—the dyes were completely decomposed within 5–9 min. Furthermore, a comparison study revealed that the CoFe2O4/CdS nanocomposite is a more efficient sonocatalyst than pure CdS; thus, adopting the nanocomposite approach is an excellent means to improve the sonoactivity of CdS. Moreover, the magnetic properties displayed by the CoFe2O4/CdS nanocomposite allow easy retrieval of the catalyst from the reaction mixture for subsequent uses.

Synthesis, antifungal activities and molecular docking studies of novel 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl dithiocarbamates

A series of 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl) propyl dithiocarbamates as new analogs of fluconazole were synthesized and their antifungal activities were evaluated. Among these compounds, 2a-f and 3a-q exhibited higher activities than fluconazole against nearly all fungi tested except Aspergillus fumigatus. Noticeably, the in vitro biological activities of 2b, 3a, 3c, 3h-k, and 3o-q against Candida species were much better than those of fluconazole and ketoconazole. Also, 2a-d, 3a-d, 3e-f, 3h-k, 3p and 3q showed higher activities against A. fumi than fluconazole. Computational docking experiments indicated that the inhibition of CYP51 involved a coordination bond with iron of the heme group, the hydrophilic H-bonding region, the hydrophobic region, and the narrow hydrophobic cleft.