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α-(N-ethyl-N-benzylamino)-3,4-dimethoxyacetophenone is a complex organic chemical compound with the molecular formula C20H24NO3. It is a derivative of acetophenone, featuring a benzylamine group attached to the alpha carbon, and two methoxy groups on the aromatic ring at the 3rd and 4th positions. α-(N-ethyl-N-benzylamino)-3,4-dimethoxyacetophenone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving the substitution of functional groups and the formation of new carbon-carbon or carbon-nitrogen bonds. The compound's properties, such as its solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic chemistry.

78095-21-3

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78095-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78095-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,9 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78095-21:
(7*7)+(6*8)+(5*0)+(4*9)+(3*5)+(2*2)+(1*1)=153
153 % 10 = 3
So 78095-21-3 is a valid CAS Registry Number.

78095-21-3Relevant academic research and scientific papers

Dopamine Agonist Properties of N-Alkyl-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinolines

Jacob, James N.,Nichols, David E.,Kohli, Jai D.,Glock, Dana

, p. 1013 - 1015 (2007/10/02)

A series of homologous N-alkyl-4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinolines was synthesized and examined for a dopamine-like ability to dilate the renal artery.The N-methyl derivative was equipotent to the 3',4'-dihydroxy derivative of the antidepressant agent nomifensine, indicating that the 8-amino group of the latter is not essential for dopamine-like activity.The N-ethyl homologue was reduced in potency when compared to the N-methyl, and the N-n-propyl, surprisingly, was essentially devoid of activity.This was unexpected in view of the fact that in all series of dopamine-like agents reported to date, N-alkylation, when one of the alkyls was an n-propyl group, either allowed retention or enhancement of potency.

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