36954-50-4

Basic information

• Product Name: N-(4-methylphenyl)-benzamide oxime
• Synonyms: N-(4-methylphenyl)-benzamide oxime
• CAS NO: 36954-50-4
• Molecular Weight: 226.278
• Mol File: 36954-50-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4-methylphenyl)-benzamide oxime(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methylphenyl)-benzamide oxime(36954-50-4)
• EPA Substance Registry System: N-(4-methylphenyl)-benzamide oxime(36954-50-4)

Safety Data

• Hazardous Substances Data: 36954-50-4(Hazardous Substances Data)

Upstream product

• 5373-55-7 N-(4-methylphenyl)thiobenzamide 
• 622-32-2 (Z)-benzaldehyde oxime 
• 932-90-1 Benzaldoxime 
• 100-52-7 benzaldehyde 
• 932-90-1 syn-benzaldehyde oxime 
• 582-78-5 N-(4-methylphenyl)benzamide 
• 147196-11-0 3-Phenyl-4-p-tolyl-1-oxa-2,4-diaza-spiro[4.6]undeca-2,6,8,10-tetraene 
• 106-49-0 p-toluidine 
• 698-16-8 benzohydroximoyl chloride 

Downstream Products

• 111273-17-7 4-(4-methylphenyl)-3-phenyl-1,2,4-oxadiazol-5(4H)-one 
• 4300-33-8 N-(4-methylphenyl)-N'-phenylurea 
• 2963-65-7 5-methyl-2-phenyl-1H-1,3-benzimidazole 
• 141693-79-0 4-(4-methylphenyl)-3-phenyl-1,2,4-oxadiazole-5(4H)-thione 
• 14016-00-3 6-methyl-2-phenylbenzoxazole 
• 1427216-61-2 C₇₄H₁₂N₂ 
• 1018788-00-5 3,5-diphenyl-4-(4-methylphenyl)-4,5-dihydro-1,2,4,5-oxadiazaborole 
• 141693-81-4 3-phenyl-4-(p-tolyl)-1,2,4-thiadiazole-5(4H)-thione 
• 141693-80-3 3-phenyl-4-(p-tolyl)-1,2,4-thiadiazole-5(4H)-one 
• 63105-04-4 4-phenyl-3-p-tolyl-3H-[1,2,3,5]oxathiadiazole 2-oxide 

Relevant articles and documents

Synthesis and substituent effect study on 13C NMR chemical shifts of 4-(substitue-phenyl)-6-methyl-3-phenyl-4H-1,2,4-oxadiazin-5(6H)-one

The twelve novel 4-(substituted-phenyl)-6-methyl-3-phenyl-4H-1,2,4-oxadiazin-5(6H)-one derivatives were synthesized by the reactions of N-Substituted-phenyl-benzamide oximes with 2-bromopropionyl chloride. The synthesized 1,2,4-oxadiazin-5-one derivatives

FeCl3·6H2O-mediated reaction of [60]fullerene with amidoximes

A FeCl3·6H2O-mediated reaction of [60]fullerene with amidoximes for the preparation of fulleroimidazolines has been presented. This reaction shows a wide substrate scope, and the products obtained from alkyl-substituted amidoximes ar

1,3-Dipolar Cycloaddition Reactions of 2,4,6-Cycloheptatrien-1-imines with Benzonitrile Oxides Leading to 1,2,4-Oxadiazaspiroundeca-2,6,8,10-tetraenes

1,3-Dipolar cycloaddition reactions of N-aryl-2,4,6-cycloheptatrien-1-imines with p-substituted benzonitrile oxides afforded -type cycloadducts in considerable yields.A study of the substituent effect on the reaction rate revealed that the reactions proceeded through nucleophilic reactions of imines to nitrile oxides.Thermal isomerizations and addition reactions of the adducts showed that the contribution of a valence isomerization between cycloheptatriene and norcaradiene lay to the side of the cycloheptatriene form.A comparison of the UV spectra between the adduct and its derivative, which was reduced by catalytic hydrogenation, implies that the spiroconjugation between cycloheptatriene and a five-membered heterocyclic moiety causes a shift of the equilibrium.