181705-88-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
5-(3-Fluorophenyl)nicotinic acid is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to be incorporated into the development of new drugs and pesticides, enhancing their efficacy and selectivity.
Used in Molecular Imaging of the Brain:
5-(3-Fluorophenyl)nicotinic acid has been studied for its potential as a molecular imaging agent for the brain. Its ability to bind to specific receptors and structures within the brain makes it a promising candidate for diagnostic imaging, allowing for better visualization and understanding of brain function and disorders.
Used in Anti-Inflammatory Applications:
Due to its anti-inflammatory properties, 5-(3-Fluorophenyl)nicotinic acid is used as a therapeutic agent for the treatment of various inflammatory conditions. Its ability to modulate inflammatory pathways and reduce inflammation can provide relief and improve the quality of life for patients suffering from these conditions.
Used in Neurological Disorder Treatment:
5-(3-Fluorophenyl)nicotinic acid has been investigated for its potential as a treatment for various neurological disorders. Its unique structure and properties may offer new avenues for the development of therapies that can address the underlying causes of these disorders and improve patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 181705-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,7,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 181705-88:
(8*1)+(7*8)+(6*1)+(5*7)+(4*0)+(3*5)+(2*8)+(1*8)=144
144 % 10 = 4
So 181705-88-4 is a valid CAS Registry Number.
181705-88-4Relevant academic research and scientific papers
Marquais, Sophie,Arlt, Michael
, p. 5491 - 5494 (1996)
Aryl zinc bromides undergo palladium catalyzed coupling reactions to aryl bromides which are bound to a polystyrene resin via an ester linkage. Liberation of the biaryl carboxylic ester was achieved by transesterification.
