22014-89-7

Basic information

• Product Name: N,N-DIBENZYL –N-PROPYL AMINE
• Synonyms: BenzeneMethanaMine, N-(phenylMethyl)-N-propyl-
• CAS NO: 22014-89-7
• Molecular Formula: C₁₇H₂₁N
• Molecular Weight: 239.36
• Mol File: 22014-89-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N-DIBENZYL –N-PROPYL AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DIBENZYL –N-PROPYL AMINE(22014-89-7)
• EPA Substance Registry System: N,N-DIBENZYL –N-PROPYL AMINE(22014-89-7)

Safety Data

• Hazardous Substances Data: 22014-89-7(Hazardous Substances Data)

Upstream product

• 107-10-8 propylamine 
• 100-39-0 benzyl bromide 
• 802294-64-0 propionic acid 
• 103-49-1 dibenzylamine 
• 123-38-6 propionaldehyde 
• 124-38-9 carbon dioxide 
• 100-44-7 benzyl chloride 
• 50-00-0 formaldehyd 
• 75-03-6 ethyl iodide 
• 620-40-6 tribenzylamine 
• 780-25-6 N-benzylidene benzylamine 
• 35929-26-1 N,N-bis(phenylmethyl)-propionamide 
• 22014-91-1 3-(dibenzylamino)prop-1-ene 
• 60479-65-4 (S)-2-(N,N-dibenzylamino)-1-propanol 

Downstream Products

• 2032-33-9 N-benzyl-N-propylamine 
• 265669-75-8 tert-Butyl 3-(N-propyl-N-benzylamino)butanoate 
• 1374146-66-3 C₃₄H₄₀N₂ 

Relevant articles and documents

Direct Reductive Amination of Carbonyl Compounds with H2 Using Heterogeneous Catalysts in Continuous Flow as an Alternative to N-Alkylation with Alkyl Halides

A general continuous-flow procedure for direct reductive amination of secondary and primary amines with aromatic and aliphatic aldehydes as well as ketones is reported. The use of hydrogen gas and commercially available Pt/C as a heterogeneous catalyst is a key. In addition to exhibiting an excellent functional group tolerance, this method allows the fast formation of C?N bonds without production of any hazardous chemical waste. Applications to the synthesis of key intermediates toward active pharmaceutical ingredients (Donepezil and Arformoterol/Tamsulosin) are also described. (Figure presented.).

Synthetic and theoretical investigation on the one-pot halogenation of β-amino alcohols and nucleophilic ring opening of aziridinium ions

Aziridinium ions are useful reactive intermediates for the synthesis of enantiomerically enriched building blocks. However, N,N-dialkyl aziridinium ions are relatively underutilized in the synthesis of optically active molecules as compared to other three

Novel synthesis of N-alkyl amines from tandem coupling of either methylamine or nitroalkane with aldehyde

A novel tandem strategy for coupling of either methylamine or nitroalkane with aldehyde has been developed. This is the first demonstration that methylamine or nitroalkane is used as a methylation reagent, fabricating N-alkyl amines. The active Pt NWs allow for the selective preparation of a series of N-alkyl amines with good to excellent yields under mild and environmentally friendly conditions.