57535-59-8

Basic information

• Product Name: N-(3,4-dimethoxybenzyl)-1-(3,4-dimethoxyphenyl)methanimine
• Synonyms: N-(3,4-dimethoxybenzyl)-1-(3,4-dimethoxyphenyl)methanimine
• CAS NO: 57535-59-8
• Molecular Weight: 315.369
• Mol File: 57535-59-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: N-(3,4-dimethoxybenzyl)-1-(3,4-dimethoxyphenyl)methanimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,4-dimethoxybenzyl)-1-(3,4-dimethoxyphenyl)methanimine(57535-59-8)
• EPA Substance Registry System: N-(3,4-dimethoxybenzyl)-1-(3,4-dimethoxyphenyl)methanimine(57535-59-8)

Safety Data

• Hazardous Substances Data: 57535-59-8(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 5763-61-1 3,4-dimethoxybenzylamine 

Downstream Products

• 1167430-59-2 C₁₉H₂₂NO₅⁽¹⁺⁾ 
• 1400942-44-0 [1,1′-biphenyl]-4-yl bis(3,4-dimethoxybenzyl)sulfamate 
• 1400942-40-6 4-bromophenyl bis(2,4-dimethoxybenzyl)sulfamate 
• 774539-27-4 2,6-di-(3'-triisopropylsilyloxypropoxy)-4,8-bis(di-N,N-(3',4'-dimethoxybenzyl)amino)pyrimido[5,4-d]pyrimidine 
• 774539-28-5 2,6-di-(3'-hydroxypropoxy)-4,8-bis(di-N,N-(3',4'-dimethoxybenzyl)amino)pyrimido[5,4-d]pyrimidine 
• 270920-53-1 2,6-di-(2'-triisopropylsilyloxyethoxy)-4,8-bis(di-N,N-(3',4'-dimethoxybenzyl)amino)pyrimido[5,4-d]pyrimidine 
• 270920-54-2 2,6-di-(2'-hydroxyethoxy)-4,8-bis(di-N,N-(3',4'-dimethoxybenzyl)amino)pyrimido[5,4-d]pyrimidine 
• 270920-52-0 2,6-dichloro-4,8-bis-[di-N,N-(3',4'-dimethoxybenzyl)amino]pyrimido[5,4-d]pyrimidine 
• 5634-21-9 N,N-bis-(3,4-dimethoxybenzyl)amine 

Relevant articles and documents

Switchable activity of a Ru catalyst bearing an annulated mesoionic carbene ligand for oxidation of primary amines

The catalytic activity of a Ru complex 1, bearing a fused π-conjugated imidazo[1,2–a][1,8]naphthyridine-based mesoionic carbene (MIC) ligand, is examined for the oxidation of primary amines. Complex 1 affords nitrile or imine depending on the nature of th

Selective Acceptorless Dehydrogenation of Primary Amines to Imines by Core–Shell Cobalt Nanoparticles

Core–shell nanocatalysts are attractive due to their versatility and stability. Here, we describe cobalt nanoparticles encapsulated within graphitic shells prepared via the pyrolysis of a cationic poly-ionic liquid (PIL) with a cobalt(II) chloride anion. The resulting material has a core–shell structure that displays excellent activity and selectivity in the self-dehydrogenation and hetero-dehydrogenation of primary amines to their corresponding imines. Furthermore, the catalyst exhibits excellent activity in the synthesis of secondary imines from substrates with various reducible functional groups (C=C, C≡C and C≡N) and amino acid derivatives.

Ligand controlled switchable selectivity in ruthenium catalyzed aerobic oxidation of primary amines

A ligand controlled catalytic system for the aerobic oxidation of 1° amines to nitriles and imines has been developed where the varying π-acidic feature of BIAN versus phen in the frameworks of ruthenium catalysts facilitates switchable selectivity.