1886-67-5

Basic information

• Product Name: Carbonimidic dichloride, [(4-methylphenyl)sulfonyl]-
• Synonyms: phosgene tosylimine;N-(Dichlormethylen)-toluensulfonamid;N-(dichloromethylidene)-4-methylbenzenesulfonamide;N-dichloromethylene-p-toluenesulfonamide;N-p-Toluenesulfonyl isocyanide dichloride;N-Dichloromethylene-4-methyl-benzenesulfonamide;(toluene-4-sulfonyl)-carbonimidic acid dichloride
• CAS NO: 1886-67-5
• Molecular Formula: C8H7Cl2NO2S
• Molecular Weight: 252.121
• Mol File: 1886-67-5.mol

Chemical Properties

• Melting Point: 80 - 83 °C
• Boiling Point: 116-118 °C(Press: 0.01 Torr)
• Density: 1.43±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Carbonimidic dichloride, [(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonimidic dichloride, [(4-methylphenyl)sulfonyl]-(1886-67-5)
• EPA Substance Registry System: Carbonimidic dichloride, [(4-methylphenyl)sulfonyl]-(1886-67-5)

Safety Data

• Hazardous Substances Data: 1886-67-5(Hazardous Substances Data)

Upstream product

• 2651-15-2 N-[bis(methylthio)methylene]-p-toluenesulfonamide 

Downstream Products

• 65159-15-1 4,4'-(toluene-4-sulfonylcarbonimidoyl)-bis-morpholine 
• 37761-81-2 2-(4-methoxy-phenyl)-3-phenyl-5-(toluene-4-sulfonylamino)-[1,3,4]oxadiazolium betaine 
• 35607-95-5 N-(3-phenyl-[1,4,2]dioxazol-5-ylidene)-toluene-4-sulfonamide 
• 35607-99-9 N-(3-phenyl-[1,4,2]oxathiazol-5-ylidene)-toluene-4-sulfonamide 
• 14631-89-1 N-(5-m-tolyl-[1,3,4]oxadiazol-2-yl)-toluene-4-sulfonamide 
• 14631-88-0 N-(5-p-tolyl-[1,3,4]oxadiazol-2-yl)-toluene-4-sulfonamide 
• 69746-64-1 N-(5,6-Dichloro-1H-benzoimidazol-2-yl)-4-methyl-benzenesulfonamide 
• 397247-79-9 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-4-methoxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 
• 611180-18-8 4-methyl-N-(1,4,6-trimethyl-1H-imidazo[4,5-c]pyridin-2-yl)-benzenesulfonamide 
• 397247-78-8 6,7-dihydro-6-(2,3,5,6-tetrahydropyran-2-yl)oxy-9-tosylaminopyrido[3',2':4,5]pyrrolo[1,2-c]pyrimidine 

Relevant articles and documents

Generation and reactivity of 2-Amido-1,3-diaminoallyl cations: Cyclic guanidine annulations via net (3 + 2) and (4 + 3) cycloadditions

Toward a method for direct conversion of alkenes to cyclic guanidines, we report that 1,3-dipolar cycloadditions of 2-Amido-1,3-diamino allylic cations with alkenes provide a new method for direct cyclic guanidine annulation. Generated under oxidative con

Syntheses of two potential food mutagens

The syntheses of the potential heterocyclic amine food mutagens 1,4,6-trimethyl-2-aminoimidazo[4,5-c]pyridine and 1,5,7-trimethyl-2 -aminoimidazo [4,5-b]pyridine are described.