52853-20-0

Basic information

• Product Name: Methanaminium, N-methyl-N-(phenylmethylene)-, chloride
• CAS NO: 52853-20-0
• Molecular Formula: C9H12N.Cl
• Molecular Weight: 169.654
• Mol File: 52853-20-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Methanaminium, N-methyl-N-(phenylmethylene)-, chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Methanaminium, N-methyl-N-(phenylmethylene)-, chloride(52853-20-0)
• EPA Substance Registry System: Methanaminium, N-methyl-N-(phenylmethylene)-, chloride(52853-20-0)

Safety Data

• Hazardous Substances Data: 52853-20-0(Hazardous Substances Data)

Upstream product

• 13880-55-2 N,N,N',N'-tetramethyl-C-phenylmethanediamine 
• 129164-52-9 chloro(dimethylamino)-o-tolylarsine 
• 100-52-7 benzaldehyde 
• 124-40-3 dimethyl amine 
• 75-36-5 acetyl chloride 
• 68-12-2 N,N-dimethyl-formamide 
• 71-43-2 benzene 

Downstream Products

• 112881-42-2 5,6,8,9-Tetrahydro-7-phenylquino<8,7-b><1,10>phenanthroline 
• 148066-23-3 7,8,13,14-Tetrahydro-6-phenylquino<8,7-k><1,8>phenanthroline 
• 94318-23-7 2-(Dimethylaminophenylmethyl)cyclohexanone 
• 39487-54-2 1-((dimethylamino)(phenyl)methyl)naphthalen-2-ol 
• 35173-74-1 3,3'-bis-indolyl(phenyl)methane 
• 347859-82-9 6-(dimethylaminophenylmethyl)-5-hydroxy-naphthalene-1-sulfonic acid amide 
• 348136-62-9 3-(dimethylaminophenylmethyl)-1H-indole-2-carboxylic acid ethyl ester 
• 347896-88-2 dimethyl-[phenyl-(1-phenyl-1H-pyrrol-2-yl)-methyl]-amine 
• 178413-47-3 6-Phenylquino<8,7-k><1,8>phenanthroline 

Relevant articles and documents

Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides

The development of the frustrated Lewis pair catalyzed hydrogenation of tertiary and secondary amides is reviewed. Detailed insight into our strategies in order to overcome challenges during the reaction development process is provided. Furthermore, the d

Substituted 1 and 2 naphthol mannich bases

The invention relates to substituted 1 and 2 naphthol Mannich bases, a method for the production thereof, medicaments containing said compounds and the use of said compounds in the production of medicaments.

Towards phase-transfer catalysts with a chiral anion: Inducing asymmetry in the reactions of cations

The ability of chiral anions, for example bis[1,1′-bi-2-naphtholato]borate, to induce asymmetry in the reactions of prochiral cations was investigated. Ion-pairing of a borate anion with an aziridinium ion was demonstrated by NMR spectroscopy. The additio