967-13-5

Basic information

• Product Name: N-(α-naphthyl)-4-nitrobenzylimine
• Synonyms: N-(α-naphthyl)-4-nitrobenzylimine
• CAS NO: 967-13-5
• Molecular Weight: 276.294
• Mol File: 967-13-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-(α-naphthyl)-4-nitrobenzylimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(α-naphthyl)-4-nitrobenzylimine(967-13-5)
• EPA Substance Registry System: N-(α-naphthyl)-4-nitrobenzylimine(967-13-5)

Safety Data

• Hazardous Substances Data: 967-13-5(Hazardous Substances Data)

Upstream product

• 134-32-7 1-amino-naphthalene 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 135569-44-7 trans-1-α-naphthyl-3-(methylphenylamino)-4-(p-nitrophenyl)-2-azetidinone 
• 83772-66-1 4-aminobenzylidene-α-naphthylamine 

Relevant articles and documents

A thermal study of some Schiff bases derivative of α-napthylamine

Thermal analyses of some Schiff bases, derivative of α-napthylamine, were performed by the DSC, TG and DTA techniques. The thermograms were used to determine various kinetic parameters, such as the order of degradation (n), energy of activation (E), frequ

Analgesic, anti-inflammatory activity and docking study of 2-(substituted phenyl)-3-(naphthalen- 1-yl)thiazolidin-4-ones

A potential analgesic and anti-inflammatory activities have been reported in 4-thiazolidinone analogs as well as some drugs bearing naphthyl moiety such as naproxen. Thus a reported series of 2-(substituted phenyl)-3-(naphthalen-1-yl)thiazolidin-4- ones (

Synthesis of optically active 1,2,3-trisubstituted azetidines employing an organocatalytic approach with L-proline

A concise organocatalytic approach towards optically active 1,2,3-trisubstituted azetidines, including a study of the scope and limitations of the synthetic sequence, is reported. The synthesis comprises the one-pot L-proline promoted three-component reac