46734-13-8

Basic information

• Product Name: Benzenamine, N,N-dimethyl-4-(phenylmethyl)-
• CAS NO: 46734-13-8
• Molecular Formula: C15H17N
• Molecular Weight: 211.307
• Mol File: 46734-13-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzenamine, N,N-dimethyl-4-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N,N-dimethyl-4-(phenylmethyl)-(46734-13-8)
• EPA Substance Registry System: Benzenamine, N,N-dimethyl-4-(phenylmethyl)-(46734-13-8)

Safety Data

• Hazardous Substances Data: 46734-13-8(Hazardous Substances Data)

Upstream product

• 64-18-6 formic acid 
• 129-73-7 bis(4-dimethylaminophenyl)phenylmethane 
• 141-53-7 sodium formate 
• 510-13-4 1,1-bis(4-dimethylaminophenyl)-1-phenyl-methanol 
• 13541-33-8 4-N,N-dimethylaminobenzyl methyl ether 
• 857005-73-3 2-(4-dimethylamino-benzyl)-benzoic acid 
• 3204-68-0 benzyldimethylphenylammonium chloride 
• 29546-14-3 4-((1H-benzo[d][1,2,3]triazol-1-yl)methyl)-N,N-dimethylaniline 
• 100-58-3 phenylmagnesium bromide 
• 825-85-4 N,N-dimethyl-p-toluidine N-oxide 
• 71-43-2 benzene 
• 7494-77-1 4-(dimethylamino)phenyl(phenyl)methanol 
• 100-10-7 4-dimethylamino-benzaldehyde 
• 586-77-6 4-bromo-N,N-dimethylaniline 

Downstream Products

• 613-42-3 4-benzylbiphenyl 
• 101-81-5 Diphenylmethane 

Relevant articles and documents

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Iridium-Catalysed Reductive Deoxygenation of Ketones with Formic Acid as Traceless Hydride Donor

An iridium-catalysed deoxygenation of ketones and aldehydes is achieved, with formic acid as hydride donor and water as co-solvent. At low catalyst loading, a number of 4-(N,N-disubstituted amino) aryl ketones are readily deoxygenated in excellent yields and chemoselectivity. Numerous functional groups, especially phenolic and alcoholic hydroxyls, secondary amine, carboxylic acid, and alkyl chloride, are well tolerable. Geminally dideuterated alkanes are obtained with up to 90% D incorporation, when DCO2D and D2O are used in place of their hydrogenative counterparts. The activating 4-(N,N-disubstituted amino)aryl groups have been demonstrated to undergo a variety of useful transformations. The deoxygenative deuterations have been used to prepare a deuterated drug molecule Chlorambucil-4,4-d2. (Figure presented.).

Super electron donor-mediated reductive desulfurization reactions

The desulfurization of thioacetals and thioethers by a pyridine-derived electron donor is described. This methodology provides efficient access to the reduced products in high yields and does not require the use of transition-metals, elemental alkali-metals, or hydrogen atom donors.