283167-06-6 Usage
Uses
Used in Pharmaceutical Drug Development:
N-(1-acetyl-4-piperidinyl)-4-fluoro-BenzaMide is used as a chemical compound in the development and testing of pharmaceutical drugs. Its unique chemical structure and potential pharmacological properties make it a promising candidate for the treatment of various neurological disorders.
Used in Serotonin Receptor Antagonism:
N-(1-acetyl-4-piperidinyl)-4-fluoro-BenzaMide is used as a serotonin receptor antagonist, which can help in the treatment of neurological disorders associated with serotonin dysregulation. Its ability to modulate serotonin receptor activity may provide therapeutic benefits in conditions such as depression, anxiety, and other mood disorders.
Used in Medicinal Chemistry Research:
N-(1-acetyl-4-piperidinyl)-4-fluoro-BenzaMide is used as a tool compound in medicinal chemistry research. Its unique structure and potential pharmacological properties make it a valuable research tool for understanding the mechanisms of action of various drugs and for the development of new therapeutic agents.
Used in Drug Discovery:
N-(1-acetyl-4-piperidinyl)-4-fluoro-BenzaMide is used in drug discovery to identify novel therapeutic agents with potential applications in treating neurological disorders and other conditions. Its unique chemical structure and pharmacological properties provide a foundation for the development of new drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 283167-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,3,1,6 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 283167-06:
(8*2)+(7*8)+(6*3)+(5*1)+(4*6)+(3*7)+(2*0)+(1*6)=146
146 % 10 = 6
So 283167-06-6 is a valid CAS Registry Number.
283167-06-6Relevant academic research and scientific papers
Amide compounds
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, (2008/06/13)
This invention relates to new amide compounds having the potentiation of the cholinergic activity, etc., and represented by general formula [I]. wherein R1 is acyl, R2 is lower alkyl, etc., A is a single bond, ?or —SO2—, E
