56108-06-6

Basic information

• Product Name: Benzenecarboximidic acid, 4-methyl-, methyl ester
• CAS NO: 56108-06-6
• Molecular Formula: C9H11NO
• Molecular Weight: 149.192
• Mol File: 56108-06-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidic acid, 4-methyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidic acid, 4-methyl-, methyl ester(56108-06-6)
• EPA Substance Registry System: Benzenecarboximidic acid, 4-methyl-, methyl ester(56108-06-6)

Safety Data

• Hazardous Substances Data: 56108-06-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 104-85-8 para-methylbenzonitrile 

Downstream Products

• 104-85-8 para-methylbenzonitrile 
• 619-55-6 para-methylbenzamide 
• 18370-11-1 N-methyl-p-methylbenzamide 
• 6726-45-0 2,4,6-tris(p-tolyl)-1,3,5-triazine 
• 2564-56-9 (R)-2-p-tolyl-4,5-dihydro-thiazole-4-carboxylic acid methyl ester 
• 52630-09-8 4-Methyl-monoselenobenzoesaeure-O-methylester 
• 32997-17-4 (5Z)-2-(4-methylphenyl)-5-(phenylmethylidene)-3,5-dihydro-4H-imidazol-4-one 
• 118543-77-4 1-[1-Methoxy-1-p-tolyl-meth-(Z)-ylidene]-3-phenyl-urea 
• 118543-75-2 1-Ethyl-3-[1-methoxy-1-p-tolyl-meth-(Z)-ylidene]-urea 
• 24239-18-7 2-<4-(bromomethyl)phenyl>benzothiazole 
• 16112-21-3 2-(4-methylphenyl)-1,3-benzothiazole 
• 75889-62-2 fostedil 
• 118543-61-6 6-amino-5-cyano-4-(4-methylphenyl)-1-phenyl-2(1H)-pyrimidinone 
• 118543-64-9 2,4-Dioxo-3-phenyl-6-p-tolyl-1,2,3,4-tetrahydro-pyrimidine-5-carbonitrile 

Relevant articles and documents

Flow rhodaelectro-catalyzed alkyne annulations by versatile C-H Activation: Mechanistic support for rhodium(III/IV)

A flow-metallaelectro-catalyzed C-H activation was realized in terms of robust rhodaelectro-catalyzed alkyne annulations. To this end, a modular electro-flow cell with a porous graphite felt anode was designed to ensure efficient turnover. Thereby, a variety of C-H/N-H functionalizations proved amenable for alkyne annulations with high levels of regioselectivity and functional group tolerance, viable in both an inter- or intramolecular manner. The electro-flow C-H activation allowed easy scale up, while in-operando kinetic analysis was accomplished by online flow-NMR spectroscopy. Mechanistic studies suggest an oxidatively induced reductive elimination pathway on rhodium(III) in an electrocatalytic regime.