139392-84-0

Basic information

• Product Name: Phosphonic acid, [[(diphenylmethylene)amino]methyl]-, bis(1,1-dimethylethyl) ester
• CAS NO: 139392-84-0
• Molecular Formula: C22H30NO3P
• Molecular Weight: 387.459
• Mol File: 139392-84-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [[(diphenylmethylene)amino]methyl]-, bis(1,1-dimethylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [[(diphenylmethylene)amino]methyl]-, bis(1,1-dimethylethyl) ester(139392-84-0)
• EPA Substance Registry System: Phosphonic acid, [[(diphenylmethylene)amino]methyl]-, bis(1,1-dimethylethyl) ester(139392-84-0)

Safety Data

• Hazardous Substances Data: 139392-84-0(Hazardous Substances Data)

Upstream product

• 1013-88-3 Benzophenone imine 
• 178676-12-5 aminomethylphosphonic acid di-tert-butyl ester 

Downstream Products

• 139392-87-3 [1-(Benzhydrylidene-amino)-3-bromo-but-3-enyl]-phosphonic acid di-tert-butyl ester 
• 139392-85-1 [1-(Benzhydrylidene-amino)-ethyl]-phosphonic acid di-tert-butyl ester 
• 139392-92-0 4-(Benzhydrylidene-amino)-4-(di-tert-butoxy-phosphoryl)-butyric acid methyl ester 
• 139392-93-1 [1-(Benzhydrylidene-amino)-3-cyano-propyl]-phosphonic acid di-tert-butyl ester 
• 139392-89-5 [1-(Benzhydrylidene-amino)-but-3-ynyl]-phosphonic acid di-tert-butyl ester 
• 139392-91-9 [(Benzhydrylidene-amino)-cyclopent-2-enyl-methyl]-phosphonic acid di-tert-butyl ester 
• 139392-86-2 [1-(Benzhydrylidene-amino)-but-3-enyl]-phosphonic acid di-tert-butyl ester 
• 139392-90-8 [(E)-1-(Benzhydrylidene-amino)-4-phenyl-but-3-enyl]-phosphonic acid di-tert-butyl ester 

Relevant articles and documents

A PRACTICAL SYNTHESIS OF α-AMINOPHOSPHONIC ACIDS

The preparation of diterbutyl-N (diphenylmethylene) aminomethylphosphonate 3 in four steps (42percent overall yield) from N-hydroxymethyl phthalimide 1 is described.Various α substituted α-aminophosphonic acids 5 containing functionalized unsaturated chains have been synthesized by alkylation of 3 under phase transfer catalysis with halides, Michael acceptors and palladium promoted reactions, followed by mild hydrolysis. Key words: Schiff bases of diterbutylaminomethylphosphonate; phase transfer catalysis; palladium-catalyzed allylic substitution; Michael additions.