58432-39-6

Basic information

• Product Name: Carbamimidothioic acid, N-methyl-N'-phenyl-, methyl ester
• CAS NO: 58432-39-6
• Molecular Formula: C9H12N2S
• Molecular Weight: 180.274
• Mol File: 58432-39-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Carbamimidothioic acid, N-methyl-N'-phenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamimidothioic acid, N-methyl-N'-phenyl-, methyl ester(58432-39-6)
• EPA Substance Registry System: Carbamimidothioic acid, N-methyl-N'-phenyl-, methyl ester(58432-39-6)

Safety Data

• Hazardous Substances Data: 58432-39-6(Hazardous Substances Data)

Upstream product

• 18306-26-8 1-phenyl-3-(trimethylsilylmethyl)thiourea 
• 77-78-1 dimethyl sulfate 
• 2724-69-8 1-methyl-3-phenylthiourea 
• 62-53-3 aniline 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 100-52-7 benzaldehyde 
• 104-88-1 4-chlorobenzaldehyde 

Relevant articles and documents

Cycloaddition of synthetic equivalent of nonstabilized aminonitrile ylides: A new route to amino-substituted aΔ2-imidazolines and Δ3-1,2,4-triazolines

The N-unsubstituted nonstabilized azomethine ylides generated from the desilylation of N-[(trimethylsilyl)methyl]iminium triflates undergo successful cycloaddition to strongly polarized sulfonylimines and diethyl azodicarboxylate to produce the corresponding Δ2-imidazolines and Δ3-1,2,4-triazolines together with the initial cycloadducts. The initial cycloadducts are converted to the corresponding aminonitrile ylide cycloadducts. Thus the present process provides a new route to amino-substituted Δ2-imidazolines and Δ3-1,2,4-triazolines that are otherwise relatively inaccessible.