105361-41-9

Basic information

• Product Name: N-benzyl-2-benzoyl-2-methylpropanimine
• Synonyms: N-benzyl-2-benzoyl-2-methylpropanimine
• CAS NO: 105361-41-9
• Molecular Weight: 265.355
• Mol File: 105361-41-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-2-benzoyl-2-methylpropanimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-2-benzoyl-2-methylpropanimine(105361-41-9)
• EPA Substance Registry System: N-benzyl-2-benzoyl-2-methylpropanimine(105361-41-9)

Safety Data

• Hazardous Substances Data: 105361-41-9(Hazardous Substances Data)

Upstream product

• 1750-74-9 2-benzoyl-2-methylpropanal 
• 100-46-9 benzylamine 

Downstream Products

• 116991-94-7 1-Benzyl-4-hydroxy-5,5-dimethyl-4-phenyl-piperidin-2-one 
• 116992-03-1 1-Benzyl-5,5-dimethyl-4-phenyl-5,6-dihydro-1H-pyridin-2-one 
• 34243-68-0 phenylmethanaminium benzoate 
• 78-84-2 isobutyraldehyde 
• 22483-21-2 isobutylidenebenzylamine 
• 88333-03-3 Benzyl isocyanide 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 611-70-1 phenyl isopropyl ketone 
• 451-40-1 phenyl benzyl ketone 
• 93-58-3 benzoic acid methyl ester 
• 22483-21-2 E-2-methylpropanal N-benzylimine 
• 116991-85-6 5-[(E)-Benzylimino]-3-hydroxy-4,4-dimethyl-3-phenyl-pentanoic acid methyl ester 
• 93-89-0 benzoic acid ethyl ester 

Relevant articles and documents

A NOVEL RETRO-ENE REACTION THE FRAGMENTATION OF N-BENZYL-2-BENZOYL-2-METHYLPROPANIMINE

N-benzyl-2-benzoyl-2-methylpropanimine treated with nucleophiles undergoes a fragmentation reaction that can be envisaged as a retro-ene reaction via the formation of an intermediate hemiketal.

Photochemical Reactivity of Aldimines from 2,2-Dimethyl-3-oxo-3-phenylpropanal

The syntheses of some thermally labile aldimines of 2,2-dimethyl-3-oxo-3-phenylpropanal are described.The aldimines (7a-c) are photochemically reactive and undergo fission mainly into isopropyl phenyl ketone.Several other minor products are also formed.On