6958-78-7

Upstream product

• 64-17-5 ethanol 
• 333-20-0 potassium thioacyanate 
• 98-88-4 benzoyl chloride 
• 532-55-8 Benzoyl isothiocyanate 
• 540-72-7 sodium thiocyanide 
• 41368-63-2 sodium derivative of diethyl (hydroxymethyl)phosphonate 

Downstream Products

• 25343-27-5 N'-benzoyl-N,N-diisobutylthiourea 
• 1821-33-6 N-phenyl-N'-benzoylurea 
• 883239-39-2 (Z)-1-benzoyl-3-benzyl-2-ethylisourea 
• 80465-17-4 3-ethoxy-1,5-diphenyl-1H-[1,2,4]triazole 
• 861542-41-8 N-(ethoxy-benzoylimino-methyl)-glycine 
• 62432-77-3 N-benzoyl O-ethyl isouree 
• 64-17-5 ethanol 
• 124-38-9 carbon dioxide 
• 333-20-0 potassium thioacyanate 
• 65-85-0 benzoic acid 
• 100-47-0 benzonitrile 
• 75-08-1 ethanethiol 
• 24785-86-2 3-ethoxy-5-phenyl-[1,2,4]oxadiazole 
• 62036-20-8 3-ethoxy-5-phenyl-1,2,4-triazole 

Relevant academic research and scientific papers

Theoretical studies of molecular structure and vibrational spectra of O-ethyl benzoylthiocarbamate

O-Ethyl benzoylthiocarbamate has been synthesized and characterized by elemental analysis and FT-IR. The crystal structure was determined by X-ray diffraction analysis. Title compound crystallizes in the orthorhombic space group Pna21, with Z =

Standard molar enthalpies of formation of three N-benzoylthiocarbamic-O- alkylesters

The standard molar enthalpies of combustion in oxygen of three crystalline N-benzoylthiocarbamic-O-alkylesters were measured at T=298.15 K by rotating bomb calorimetry. The standard molar enthalpy of sublimation of the three compounds were measured using

An efficient synthesis of 1,2,4-oxathiazoles from N-acylthiourea derivatives

l,2,4-Oxathiazoles have been synthesized from their precursors, the N-acylthioureas by oxidative cyclization reaction. Ring structure and the charge distribution above the ring have also been studied.

Ligand Properties of N-Acyl-thiocarbamic-O-alkylesters - A New Class of Aza-analogous 1,3-Thioxoketones

A series of six N-benzoyl-thiocarbamic-O-alkylesters (R=Me, Et, i-Pr, Benzyl, n-Hex, n-Dodec; 1-6) has been prepared and characterized.They are weak monoprotic acids.The compounds behave as fairly stable and versatile bidentate (O,S)-chelating ligands towards multivalent metal ions e.g.Ni(II), Cu(II), Pb(II) the stability constants of which have been determined in 75 volpercent dioxane/water.The molecular structure of bis(O-ethyl-N-benzoylthiocarbamato)nickel(II) 2a is presented.The coordination of the nickel atom is square planar with the two sulphur atoms in cis position.