1006-93-5

Basic information

• Product Name: Benzenecarboximidoyl chloride, N-ethyl-
• CAS NO: 1006-93-5
• Molecular Formula: C9H10ClN
• Molecular Weight: 167.638
• Mol File: 1006-93-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidoyl chloride, N-ethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidoyl chloride, N-ethyl-(1006-93-5)
• EPA Substance Registry System: Benzenecarboximidoyl chloride, N-ethyl-(1006-93-5)

Safety Data

• Hazardous Substances Data: 1006-93-5(Hazardous Substances Data)

Upstream product

• 614-17-5 N-ethylbenzamide 
• 98-88-4 benzoyl chloride 
• 7719-09-7 thionyl chloride 
• 1696-17-9 N,N-diethylbenzamide 

Downstream Products

• 1775-59-3 N-ethyl-benzimidic acid ethyl ester 
• 825-60-5 benzimidic acid ethyl ester 
• 614-17-5 N-ethylbenzamide 
• 3472-77-3 1,1,3,4,4,4-Hexachlor-1-phenyl-2-aza-buten-⁽²⁾ 
• 127040-92-0 N-Ethyl-benzimidic acid pent-4-enyl ester 
• 127040-91-9 4-(N-Ethyl-benzimidoyloxy)-2-methylene-butyric acid methyl ester 
• 127040-93-1 5-(N-Ethyl-benzimidoyloxy)-2-methylene-pentanoic acid methyl ester 
• 134589-81-4 Ethyl-[1-phenyl-hept-2-yn-(E)-ylidene]-amine 
• 220079-23-2 Ethyl-[1-phenyl-3-trimethylsilanyl-prop-2-yn-(E)-ylidene]-amine 
• 952595-20-9 3-[tricarbonyl(2,4-cyclohexadien-1-yl)iron]-5-methyl-2-phenyl-1H-pyrrole 
• 14321-27-8 N-ethylbenzylamine 
• 1365547-05-2 4-ethyl-3-methyl-1,5-diphenyl-1,4-dihydroimidazo[4,5-c]-pyrazole 
• 1365546-76-4 N'-(4-bromo-3-methyl-1-phenyl-1H-pyrazol-5-yl)-N-ethylbenzimidamide 
• 1365546-62-8 N-ethyl-N'-(3-methyl-1-phenyl-1H-pyrazol-5-yl)benzimidamide 

Relevant articles and documents

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Hydrogenation of Secondary Amides using Phosphane Oxide and Frustrated Lewis Pair Catalysis

The metal-free catalytic hydrogenation of secondary carboxylic acid amides is developed. The reduction is realized by two new catalytic reactions. First, the amide is converted into the imidoyl chloride by triphosgene (CO(OCCl3)2) using novel phosphorus(V) catalysts. Second, the in situ generated imidoyl chlorides are hydrogenated in high yields by an FLP-catalyst. Mechanistic and quantum mechanical calculations support an autoinduced catalytic cycle for the hydrogenation with chloride acting as unusual Lewis base for FLP-mediated H2-activation.

Preparation of 1,5-disubstituted tetrazoles under phase-transfer conditions

Imidoyl chlorides, obtained by common methods from a wide range of aromatic mono- and diamides, are smoothly converted to the corresponding tetrazoles in high yields by treatment with NaN3 under phase-transfer conditions.