105878-20-4

Basic information

• Product Name: Benzenecarbothioamide, 4-methoxy-N-(1-methyl-2-pyrrolidinylidene)-
• CAS NO: 105878-20-4
• Molecular Formula: C13H16N2OS
• Molecular Weight: 248.349
• Mol File: 105878-20-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioamide, 4-methoxy-N-(1-methyl-2-pyrrolidinylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioamide, 4-methoxy-N-(1-methyl-2-pyrrolidinylidene)-(105878-20-4)
• EPA Substance Registry System: Benzenecarbothioamide, 4-methoxy-N-(1-methyl-2-pyrrolidinylidene)-(105878-20-4)

Safety Data

• Hazardous Substances Data: 105878-20-4(Hazardous Substances Data)

Upstream product

• 126336-80-9 4-Methoxy-N-[1-methyl-pyrrolidin-(2E)-ylidene]-benzamide 
• 3424-93-9 4-methoxyphenylacetamide 
• 872-50-4 1-methyl-pyrrolidin-2-one 
• 2362-64-3 p-methoxythiobenzamide 

Downstream Products

• 127500-06-5 2-{[2-(4-Methoxy-phenyl)-4-(3-methylamino-propyl)-thiazol-5-yl]-phenyl-methylene}-malononitrile; hydrobromide 
• 126336-61-6 {3-[5-(4-Methoxy-phenyl)-2-(4-nitro-phenyl)-2H-[1,2,4]triazol-3-yl]-propyl}-methyl-amine; hydriodide 
• 127500-03-2 [2-(4-Methoxy-phenyl)-4-(3-methylamino-propyl)-thiazol-5-yl]-phenyl-methanone; hydrobromide 
• 132611-42-8 3-(3-methylaminopropyl)-5-(4-methoxyphenyl)-1,2,4-thiadiazole 
• 127500-05-4 2-(4-Methoxy-phenyl)-4-(3-methylamino-propyl)-thiazole-5-carbonitrile; hydrochloride 
• 127500-02-1 (3-{2-(4-Methoxy-phenyl)-5-[2-(4-nitro-phenyl)-2H-[1,2,4]triazol-3-yl]-thiazol-4-yl}-propyl)-methyl-amine; hydrochloride 
• 126336-72-9 5-{[1-(4-Methoxy-phenyl)-1-methylsulfanyl-meth-(Z)-ylidene]-amino}-1-methyl-3,4-dihydro-2H-pyrrolium; iodide 
• 127500-04-3 (4-Bromo-phenyl)-[2-(4-methoxy-phenyl)-4-(3-methylamino-propyl)-thiazol-5-yl]-methanone; hydrobromide 

Relevant articles and documents

Ring Transformations of Semicyclic 1,3-Dicarbonyl Heteroanalogs; I. Synthesis of Semicyclic N-Acyl- and N-(Aminocarbonyl)amidine Derivatives and Their Ring Transformation to 5-(ω-Aminoalkyl)-1,2,4-triazoles

The semicyclic N-(thioacyl)- or N-(aminothiocarbonyl)amidines 11 are readily available through reaction of O-methyllactims 9 or in situ generated lactam acetales 10 with aminothiocarbonyl compounds 7 or with carboxamides or ureas 8 and sulfurization of th