2742-65-6

Basic information

• Product Name: N,N-diethyl-N'-p-tolyl-thiourea
• Synonyms: N,N-diethyl-N'-p-tolyl-thiourea
• CAS NO: 2742-65-6
• Molecular Weight: 222.354
• Mol File: 2742-65-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N-diethyl-N'-p-tolyl-thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diethyl-N'-p-tolyl-thiourea(2742-65-6)
• EPA Substance Registry System: N,N-diethyl-N'-p-tolyl-thiourea(2742-65-6)

Safety Data

• Hazardous Substances Data: 2742-65-6(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 

Downstream Products

• 34587-31-0 5-phenyl-2-p-tolylimino-1,3-oxathiole 
• 660-68-4 diethyl amine hydrochloride 
• 86869-50-3 3-p-tolyl-4-phenyl-2-oxa-4-thiazoline 
• 77589-07-2 S-phenacyl-N,N-diethyl-N'-p-tolylthiourea 
• 74376-27-5 ethyl 5-methyl-2-p-tolylimino-1,3-oxathiole-4-carboxylate 
• 20044-34-2 ethyl 2-p-tolylimino-4-methyl-Δ⁴-thiazoline-5-carboxylate 
• 622-59-3 1-isothiocyanato-4-methylbenzene 
• 621-01-2 N,N'-Bis(p-tolyl)thiourea 
• 14285-68-8 decacarbonyldirhenium⁽⁰⁾ 
• 174750-11-9 [Re₂(CO)9(CH₃C₆H₄NHCSN(C₂H₅)2)] 
• 174750-13-1 [Re₂(CO)6(CH₃C₆H₄NCSN(C₂H₅)2)2] 
• 77589-09-4 [4-(4-Chloro-phenyl)-3-phenyl-3H-thiazol-(2Z)-ylidene]-p-tolyl-amine 
• 77589-08-3 (3,4-diphenyl-3H-thiazol-2-ylidene)-p-tolyl-amine 
• 1145-66-0 1-(4-methylphenyl)-3-phenylthiourea 

Relevant articles and documents

Reaction of 1,4,2-Dithiazolium Salts with Amino Compounds

Systematic studies on the behavior of 1,4,2-dithiazolium cations (1) toward various amino compounds (ammonia, aliphatic and aromatic amines, hydrazine, semicarbazide, thiosemicarbazide derivatives, etc.) were performed.The reaction pathway could be classified into three types depending on possibile three fission modes of the initially-formed adduct.The main products were 5-imino-1,4,2-dithiazole, thiourea, and 1,3,4-thiadiazole derivatives, through the three different pathways, respectively.In order to clarify the factors controlling the reaction courses, the reactions of 1 with p-substituted aniline derivatives were carried out under systematically varying conditions.The strength of bases and the polaritiy of solvents had clear influence on the reactivity.The reaction mechanism is also discussed.