59541-69-4

Basic information

• Product Name: methyl N'-cyano-N-(4-methylphenyl)imidothiocarbamate
• Synonyms: methyl N'-cyano-N-(4-methylphenyl)imidothiocarbamate;3-cyano-2-methyl-1-(p-tolyl)isothiourea
• CAS NO: 59541-69-4
• Molecular Formula: C₁₀H₁₁N₃S
• Molecular Weight: 205.28
• Mol File: 59541-69-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl N'-cyano-N-(4-methylphenyl)imidothiocarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl N'-cyano-N-(4-methylphenyl)imidothiocarbamate(59541-69-4)
• EPA Substance Registry System: methyl N'-cyano-N-(4-methylphenyl)imidothiocarbamate(59541-69-4)

Safety Data

• Hazardous Substances Data: 59541-69-4(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 10191-60-3 dimethyl N-cyanodithioiminocarbonate 
• 74-88-4 methyl iodide 

Downstream Products

• 60178-43-0 2-methyl-1-(3-phenyl-[1,2,4]oxadiazol-5-yl)-3-p-tolyl-isothiourea 
• 59566-70-0 2-methyl-1-(4-oxo-6-phenyl-4H-[1,3,5]thiadiazin-2-yl)-3-p-tolyl-isothiourea 
• 74-93-1 methylthiol 
• 106580-59-0 1-Methyl-N⁵-p-tolyl-1H-[1,2,4]triazole-3,5-diamine 
• 3929-18-8 N³-(p-tolyl)-1H-1,2,4-triazole-3,5-diamine 
• 1453125-14-8 7-amino-2-(4-methylphenylamino)-1,2,4-triazolo[1,5-a][1,3,5]triazine 

Relevant articles and documents

Inhibition of Copper Corrosion with N-Arylaminotriazoles in Aqueous Chloride Solutions and in Air

Abstract: A series of 3-(N-arylamino)-5-amino-1Н-1,2,4-triazoles were prepared by the reaction of S,S-dimethyl cyanodithioimidocarbamate with appropriate anilines. The inhibiting effect of the products on the corrosion of copper of M1 grade in acidic and neutral chloride-containing media was studied using electrochemical and accelerated electroless methods. The maximal degree of protection ensured by commercially available 3,5-diamino-1H-1,2,4-triazole and the synthesized 3-phenylamino, 3-(4-methylphenylamino), 3-(4-chlorophenylamino), and 3-(3-chlorophenylamino) derivatives of 5-amino-1Н-1,2,4-triazole reaches 70–87%. In acid solutions, the synthesized compounds show higher performance than the 3,5-diamino derivative, ensuring up to 92–96% protection. Similar results were obtained in experiments in a salt fog chamber.