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Usage

Uses

Used in Pharmaceutical Industry:
α-[2-(Diethylamino)ethyl]benzhydryl alcohol is used as a therapeutic agent for the treatment of Parkinson's disease and other movement disorders. It is administered in the form of oral tablets or liquid solution to block the action of acetylcholine, thereby reducing the tremors, muscle stiffness, and involuntary movements associated with these conditions.
Used in Neurological Treatments:
In the field of neurology, α-[2-(Diethylamino)ethyl]benzhydryl alcohol is utilized as a medication to manage the symptoms of movement disorders by modulating the neurotransmitter acetylcholine, which is integral to the regulation of muscle movements.

InChI:InChI=1/C19H25NO/c1-3-20(4-2)16-15-19(21,17-11-7-5-8-12-17)18-13-9-6-10-14-18/h5-14,21H,3-4,15-16H2,1-2H3

Upstream product

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• 119-61-9 benzophenone 
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Downstream Products

• 102700-17-4 6-diethylamino-4,4-diphenyl-hexan-3-one 
• 5558-76-9 4-diethylamino-2,2-diphenyl-butyronitrile 
• 779981-95-2 Carbonic acid 3-diethylamino-1,1-diphenyl-propyl ester 4-nitro-phenyl ester 
• 100001-06-7 diethyl-(3-hydroxy-3,3-diphenyl-propyl)-methyl-ammonium; iodide 
• 859060-24-5 diethyl-(3-chloro-3,3-diphenyl-propyl)-amine 
• 102009-54-1 N,N-diethyl-3,3-diphenylprop-2-en-1-amine 
• 115-64-0 1-cyclohexyl-3-diethylamino-1-phenyl-propan-1-ol 

Relevant academic research and scientific papers

Tuning the reducing properties of 1,2-diaryl-1,2-disodiumethanes

(Chemical Equation Presented) We investigated the reducing properties of a series of 1,2-diaryl-1,2-disodiumethanes by means of equilibration reactions. The electron-donor power of these vic-diorganometals is strongly affected by the nature of substituents present either on the aromatic ring(s) or on the carbanionic centers, and it can be correlated with their ability to delocalize the arylmethyl carbanions. These findings are supported by electrochemical analysis of the reduction behavior of the parent 1,2-diarylalkene. Applications of these results to the reduction of selected substrates are described. 2009 American Chemical Society.