90496-15-4

Upstream product

• 123-72-8 butyraldehyde 
• 64-04-0 phenethylamine 

Downstream Products

• 23068-45-3 N-Butyl-2-phenylethylamine 
• 90496-18-7 Phenethyl-(1-propyl-pentyl)-amine 
• 91406-86-9 Phenethyl-(1-propyl-hex-2-ynyl)-amine 
• 113437-13-1 1-Phenethyl-4-propyl-azetidin-2-one 
• 122137-53-5 3-Methyl-1-phenethyl-4-propyl-azetidin-2-one 
• 90496-19-8 Phenethyl-(1-phenethyl-butyl)-amine 
• 91406-87-0 Phenethyl-(1-phenylethynyl-butyl)-amine 
• 110448-88-9 (2S,5S)-1-Phenethyl-2-phenylselanylmethyl-5-propyl-pyrrolidine 
• 110448-88-9 (2S,5R)-1-Phenethyl-2-phenylselanylmethyl-5-propyl-pyrrolidine 
• 110448-83-4 Phenethyl-(1-propyl-pent-4-enyl)-amine 
• 113437-16-4 3,3-Dimethyl-1-phenethyl-4-propyl-azetidin-2-one 

Relevant academic research and scientific papers

Facile synthesis and in vitro properties of 1-alkyl- and 1-alkyl-N-propargyl-1,2,3,4-tetrahydroisoquinoline derivatives on PC12 cells

The synthesis of several 1-alkyl-1,2,3,4-tetrahydroisoquinolines, which may play an important role in Parkinson's disease, has been achieved by modified Pictet-Spengler cyclization of the formyliminium ion. The direct cytotoxicity and preventative effects

One-pot preparation of chiral beta-amino esters by rhodium-catalyzed three-components coupling reaction.

Chiral beta-amino esters are synthesized in one-pot from three components, amines, aldehydes, and ethyl bromoacetate, under the rhodium-catalyzed Reformatsky-type reaction condition, where complete diastereoselection is achieved in the nucleophilic addition step of ethyl bromoacetate to the imines prepared in