843-29-8

Basic information

• Product Name: Benzenamine, 4,4'-methylenebis[N-ethyl-
• CAS NO: 843-29-8
• Molecular Formula: C17H22N2
• Molecular Weight: 254.375
• Mol File: 843-29-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4,4'-methylenebis[N-ethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4,4'-methylenebis[N-ethyl-(843-29-8)
• EPA Substance Registry System: Benzenamine, 4,4'-methylenebis[N-ethyl-(843-29-8)

Safety Data

• Hazardous Substances Data: 843-29-8(Hazardous Substances Data)

Upstream product

• 103670-28-6 N,N'-Diethyl-N,N'-bis(p-tolylsulfonyl)-4,4'-methylendianilin 
• 74205-82-6 1-(hydroxymethyl)-1,2,4-triazole 
• 103-69-5 N-ethyl-N-phenylamine 
• 7647-01-0 hydrogenchloride 
• 50-00-0 formaldehyd 
• 5419-13-6 N,N'-diethyl-N,N'-diphenyl-methanediyldiamine 
• 74043-79-1 4,4’-methylenebis(N-p-tosylanilide) 
• 71893-15-7 C₄H₇ClHgO 
• 5293-94-7 bis(chloromethyl)mercury 
• 4348-19-0 N-ethylaniline hydrochloride 

Downstream Products

• 103670-31-1 N,N'-Bis(cyanmethyl)-N,N'-diethyl-4,4'-methylendianilin 
• 861083-89-8 bis-[4-(ethyl-nitroso-amino)-phenyl]-methane 

Relevant articles and documents

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Azamacrocycles with N-(Aminoalkyl) Side Chains: Syntheses, Metal Complexes, and Catalysis of Acyl Tranfer Reactions

Azacyclophanes containing ethylene diamine groups and open chain analogues are prepared e. g. by reactions with bromoacetonitrile and subsequent reduction.Metal complexes of the composition L*Cu4Cl8, L*Zn2Cl4, L*Ni6Cl12* 8 H2O, L*Co4(NO3)8* 16 H2O, where

Alkylidene Transfer from Monochloroalkylmercury(II) Compounds to Aromatic Amines; Selective C-Alkylation

αα-Diarylalkane derivatives have been synthesized from monochloroalkylmercury(II) compounds in a noncarbenoid alkylidene transfer reaction which takes place selectively on the aromatic ring.A mechanism is suggested for this process.Intermediate products are prepared by alternative routes to ascertain their participation in the course of the reaction.As a consequence, two different aryl groups can be successively incorporated into the alkane molecule.