15366-65-1 Usage
Uses
Used in Organic Synthesis:
5-Iodonicotinic acid is used as a building block in organic synthesis for its ability to contribute to the formation of a wide range of compounds. Its presence in the molecular structure can influence the reactivity and properties of the synthesized products, making it a versatile component in chemical reactions.
Used in Pharmaceutical Research:
In pharmaceutical research, 5-Iodonicotinic acid is utilized as a precursor in the synthesis of pharmaceutical drugs. Its unique iodine-containing structure can be key in the development of new medications, potentially enhancing their efficacy or targeting specific biological pathways.
Used in Agrochemicals:
5-Iodonicotinic acid is also used as a precursor in the synthesis of agrochemicals, where it may contribute to the development of new pesticides or other agricultural chemicals. Its role in these compounds can be crucial for improving crop protection and yield.
Used in Therapeutic Applications:
5-Iodonicotinic acid has been studied for its potential therapeutic properties, indicating its use in the treatment of various diseases and disorders. The presence of iodine may offer specific benefits in medical treatments, although further research is necessary to fully understand its implications in healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 15366-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15366-65:
(7*1)+(6*5)+(5*3)+(4*6)+(3*6)+(2*6)+(1*5)=111
111 % 10 = 1
So 15366-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4INO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,(H,9,10)
15366-65-1Relevant academic research and scientific papers
A unified synthetic strategy for the indolopyridine alkaloid group
Lavilla, Rodolfo,Gullón, Francisco,Bosch, Joan
, p. 373 - 378 (2007/10/03)
Thermal or acetyl chloride induced cyclization of bromoenamide 10 affords the pentacyclic derivative 12 with high yield and regioselectivity. From this common synthetic intermediate, palladium-catalyzed reactions allow the total synthesis of indolopyridin
