31124-88-6

Basic information

• Product Name: 3-(4-methoxyphenyl)-1,1-dimethylthiourea
• Synonyms: methanethiol, 1-(dimethylamino)-1-[(4-methoxyphenyl)imino]-, (Z)-; N'-(4-Methoxyphenyl)-N,N-dimethylcarbamimidothioic acid
• CAS NO: 31124-88-6
• Molecular Formula: C₁₀H₁₄N₂OS
• Molecular Weight: 210.296
• Mol File: 31124-88-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 296.4°C at 760 mmHg
• Flash Point: 133°C
• Density: 1.18g/cm³
• Vapor Pressure: 0.00144mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 3-(4-methoxyphenyl)-1,1-dimethylthiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)-1,1-dimethylthiourea(31124-88-6)
• EPA Substance Registry System: 3-(4-methoxyphenyl)-1,1-dimethylthiourea(31124-88-6)

Safety Data

• Hazardous Substances Data: 31124-88-6(Hazardous Substances Data)

Upstream product

• 137-26-8 Thiram 
• 104-94-9 4-methoxy-aniline 
• 124-40-3 dimethyl amine 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 

Downstream Products

• 75105-03-2 6-methoxy-N,N-dimethylbenzo[d]thiazol-2-amine 
• 1329429-73-3 3-(4-methoxyphenyl)-1,1-dimethyl-2-phenyl-isothiourea 
• 1329429-71-1 N'-(4-methoxyphenyl)-N,N-dimethyl-2-phenylsulfanyl-benzamidine 
• 41875-31-4 (CO)3Fe(SCN(CH₃)2NHC₆H₄OCH₃)2 
• 312727-41-6 dimethyl-[6-(2-piperidino-ethoxy)-benzothiazol-2-yl]-amine 
• 95-27-2 Dimazole 
• 943-04-4 2-dimethylamino-benzothiazol-6-ol 
• 86671-69-4 N¹-(p-methoxyphenyl)-N³-(3-mercapto-5-methyl)-1,2,4-triazol-4-yl thiourea 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 

Relevant articles and documents

Insertion of arynes into thioureas: A new amidine synthesis

Arynes, generated from trimethylsilyl phenyltriflate precursors, have been found to react with thioureas via a formal π-insertion into the C=S bond. The reaction contrasts with that of ureas, which proceeds via benzyne σ-insertion into the C-N bond, and r

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.