75509-56-7

Upstream product

• 506-59-2 N,N-dimethylammonium chloride 
• 75509-55-6 2-<1-(p-methoxyphenyl)-3-oxopropyl>-1,3-dioxolan 
• 75509-59-0 (+/-)-NN-dimethyl-4-(ethylenedioxy)-3-(p-methoxyphenyl)butyramide 
• 53484-50-7 p-methoxycinnamyl alcohol 
• 85624-03-9 (+/-)-α-allyl-α-(p-methoxyphenyl)acetonitrile 
• 85624-04-0 (+/-)-α-allyl-α-(p-methoxyphenyl)acetaldehyde 
• 75523-05-6 (+/-)-NN-dimethyl-3-(p-methoxyphenyl)pent-4-enamide 
• 75509-54-5 2-<1-(p-methoxyphenyl)but-3-enyl>-1,3-dioxolan 
• 104-47-2 p-methoxybenzylnitrile 
• 75509-61-4 (+/-)-NN-dimethyl-4-oxo-3-(p-methoxyphenyl)butyramide 

Downstream Products

• 34603-52-6 1-[2-(dimethylamino)ethyl]-4'-methoxy-2,3-dihydro-[1,1′-biphenyl]-4(1H)-one 
• 75523-04-5 2-(p-methoxyphenyl)-4-(NN-dimethylamino)butanal 

Relevant academic research and scientific papers

Applications of Substituted Arylacetaldehydes in the Total Synthesis of seco-Mesembrane Alkaloids. Part 1. The Total Synthesis of (+/-)-O-Methyljoubertiamine

The substituted arylacetaldehyde 2-(p-methoxyphenyl)-5-dimethylaminobutanol (1a) is shown to serve as a precursor in the total synthesis of the seco-mesembrane alkaloid (+/-)-O-methyljoubertiamine (2; R1R2=O, R3=Me, Δ