40339-47-7

Basic information

• Product Name: Benzenamine, N-[(4-methoxyphenyl)methylene]-, (Z)-
• CAS NO: 40339-47-7
• Molecular Formula: C14H13NO
• Molecular Weight: 211.263
• Mol File: 40339-47-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-[(4-methoxyphenyl)methylene]-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-[(4-methoxyphenyl)methylene]-, (Z)-(40339-47-7)
• EPA Substance Registry System: Benzenamine, N-[(4-methoxyphenyl)methylene]-, (Z)-(40339-47-7)

Safety Data

• Hazardous Substances Data: 40339-47-7(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 62-53-3 aniline 

Downstream Products

• 57427-78-8 (4Z)-4-(4-methoxybenzylidene)-2-phenyl-oxazolin-5-one 
• 57880-71-4 3,3-dichloro-4-(p-methoxyphenyl)-1-phenyl-2-azetidinone 
• 7380-78-1 4-(phenylethynyl)anisole 
• 101067-86-1 (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one 
• 182824-73-3 (3R,4S)-4-(4-Benzyloxy-phenyl)-3-[(S)-2-(4-fluoro-phenoxy)-1-hydroxy-ethyl]-1-(4-fluoro-phenyl)-azetidin-2-one 

Relevant articles and documents

Unlocking the catalytic potential of tris(3,4,5-trifluorophenyl)borane with microwave irradiation

The catalytic activity of tris(3,4,5-trifluorophenyl)borane has been explored in the 1,2-hydroboration reactions of unsaturated substrates. Under conventional conditions, the borane was found to be active only in the hydroboration of aldehyde, ketone and imine substrates, with alkenes and alkynes not being reduced effectively. The use of microwave irradiation on the other hand has permitted alkenes and alkynes to be hydroborated in good yields.

Poly(ethylene glycol) supported liquid-phase synthesis of 1,2,4-oxadiazolines

The liquid-phase synthesis of oxadiazolines via 1,3-dipolar cycloaddition reaction on poly(ethylene glycol) support (PEG) is described. 1,3-Dipolar cycloadditions of nitrile oxide generated in situ on soluble polymer with a variety of imines provided a li

A convenient synthetic approach to alpha-amino-beta-lactam synthesis promoted by phenyl dichlorophosphate reagent

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