70509-09-0

Basic information

• Product Name: N-(diphenylmethylene)-etheneamine
• Synonyms: N-(diphenylmethylene)-etheneamine
• CAS NO: 70509-09-0
• Molecular Weight: 207.275
• Mol File: 70509-09-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(diphenylmethylene)-etheneamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(diphenylmethylene)-etheneamine(70509-09-0)
• EPA Substance Registry System: N-(diphenylmethylene)-etheneamine(70509-09-0)

Safety Data

• Hazardous Substances Data: 70509-09-0(Hazardous Substances Data)

Upstream product

• 21160-02-1 benzophenone O-acetyl oxime 
• 7486-35-3 tri-n-butyl(vinyl)tin 
• 80500-07-8 2-(diphenylmethyleneamino)ethanol 
• 119-61-9 benzophenone 
• 65231-78-9 N'-(Diphenylmethylen)-N,N-dimethyl-1,2-ethandiamin 
• 1013-88-3 Benzophenone imine 

Relevant articles and documents

Synthesis of the Aminocyclitol Core of Jogyamycin via an Enantioselective Pd-Catalyzed Trimethylenemethane (TMM) Cycloaddition

The use of β-nitroenamines as a new class of acceptors in the enantioselective Pd-catalyzed trimethylenemethane cycloaddition afforded differentiated 1,2-dinitrogen bearing cyclopentanes with three contiguous stereocenters. The utility of these acceptors was demonstrated with the efficient construction of the core of jogyamycin and aminocyclopentitols. Further elaboration of the cycloadducts provided a concise synthetic approach toward joygamycin.

N-substituted imines by the copper-catalyzed N-imination of boronic acids and organostannanes with O-acyl ketoximes

Catalytic quantities of copper(I) or copper(II) sources catalyze the N-imination of boronic acids and organostannanes through reaction with oxime O-carboxylates under nonbasic conditions. This method tolerates various functional groups and takes place efficiently using aryl, heteroaryl, and alkenyl boronic acids and stannanes.