4949-93-3

Usage

InChI:InChI=1/C14H14N2S/c1-16(13-10-6-3-7-11-13)14(17)15-12-8-4-2-5-9-12/h2-11H,1H3,(H,15,17)

Upstream product

• 64-17-5 ethanol 
• 103-72-0 phenyl isothiocyanate 
• 100-61-8 N-methylaniline 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 13023-88-6 methyl-triphenyl-urea 
• 3111-89-5 O-ethyl-N-phenylthiocarbamate 
• 100-61-8 N-methylaniline 
• 103-85-5 monophenylthiourea 
• 103-72-0 phenyl isothiocyanate 
• 198488-64-1 methyl N-methyl-N,N′-diphenylcarbamimidothioate 
• 32189-59-6 N-methyl-N,N'-diphenylformamidine 
• 55712-18-0 2-(N-methyl-anilino)-4,6-dioxo-3,5-diphenyl-5,6-dihydro-4H-[1,3]thiazinium betaine 
• 611-92-7 1,3-dimethyl-1,3-diphenylurea 
• 62603-94-5 methyl N-methyl-N-phenyldithiocarbamate 
• 22695-18-7 N,N-di-o-tolylthiourea 
• 62-53-3 aniline 
• 102-08-9 N,N-diphenylthiourea 

Relevant academic research and scientific papers

Method for preparing aryl isothiourea

The invention discloses a method for preparing aryl isothiourea, wherein hydride is suspended in a solvent, and thiourea is sequentially added. O diiodo benzene followed by reaction to prepare aryl isothiosemicarbazone. The isothiourea structure is widely

Hydroamination and Hydrophosphination of Isocyanates/Isothiocyanates under Catalyst-Free Conditions

Symmetrical and unsymmetrical N,N’-disubstituted as well as trisubstituted ureas/thioureas by the hydroamination of isocyanates/isothiocyanates, and various phosphathioureas by the hydrophosphination of isothiocyanates have been synthesized in good to excellent yields under catalyst-free and mild conditions. This protocol is also applicable for the efficient synthesis of chiral ureas and thioureas and common herbicides, such as fenuron and monuron.

Photocatalytic synthesis of unsymmetrical thiourea derivativesviavisible-light irradiation using nitrogen-doped ZnO nanorods

An efficient, mild, and environmentally friendly route has been developed for the synthesis of unsymmetrical thiourea derivatives in moderate yields by the reaction of tertiary aromatic and aliphatic amines with phenyl-iso-thiocyanate in the presence of N-ZnO as a photocatalyst under visible-light irradiation. This method provides a pathway to activate the tertiary aromatic and aliphatic aminesviaC-N bond cleavage.

Facile Synthesis of Some Chlorinated and Heteroatom-Rich Monocyclic β-Lactams via the Staudinger Reaction of Acyclic S -Alkylisothioureas

The optimized preparation of a rare class of highly functionalized (chlorinated and heteroatom-rich) monocyclic β-lactams by the Staudinger reaction of reactive acyclic S-alkylisothioureas with dichloroketene is presented. The use of acyclic S-alkylisothi

Studies on Aryl- and Diaryl-thioureas and their Insecticidal Activity

Certain aryl- and diaryl-thioureas having insecticidal activity have been prepared.Their insecticidal property has been evaluated on Sitophilus oryzae (Linn.). 13C NMR spectrum of 1,3-diphenylthiourea has been studied.