Product Name:2-(1H-indol-3-yl)nicotinonitrile

IUPAC Name:2-(1H-indol-3-yl)pyridine-3-carbonitrile

CAS:3191-30-8
Molecular Formula:C14H9N3
Purity:95%
Catalog Number:CM148845
Molecular Weight:219.25

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CM148845-1g 3-4 Weeks ǶȐŵ

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Product Details

CAS NO:3191-30-8
Molecular Formula:C14H9N3
Melting Point:-
Smiles Code:N#CC1=C(C2=CNC3=C2C=CC=C3)N=CC=C1
Density:
Catalog Number:CM148845
Molecular Weight:219.25
Boiling Point:
MDL No:MFCD11915916
Storage:

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Indoles
Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.
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Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

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Product Overview 2-(1H-indol-3-yl)nicotinonitrile is a chemical compound that belongs to the class of heterocyclic compounds. It is a derivative of indole, a naturally occurring compound found in many plants. This compound has gained significant attention in the scientific community due to its potential applications in drug discovery and development.
Synthesis and Application The synthesis of 2-(1H-indol-3-yl)nicotinonitrile involves the reaction of 3-cyanoindole with nicotinaldehyde in the presence of a base. The reaction proceeds through a condensation reaction, resulting in the formation of the desired product. The yield of the product can be improved by optimizing the reaction conditions, such as the choice of solvent, temperature, and reaction time. 2-(1H-indol-3-yl)nicotinonitrile has shown promising results in scientific research, particularly in drug discovery and development. It has been reported to exhibit a wide range of pharmacological activities, including anti-inflammatory, anti-cancer, anti-viral, and anti-bacterial properties. The compound has been tested against various cancer cell lines, and it has shown potent cytotoxic activity. It has also been found to inhibit the growth of certain viruses and bacteria.
Future Directions There are several future directions for the research on 2-(1H-indol-3-yl)nicotinonitrile. One area of interest is the development of novel drugs based on this compound. The potent pharmacological activity of 2-(1H-indol-3-yl)nicotinonitrile makes it a promising candidate for drug discovery. Another area of interest is the elucidation of the mechanism of action of this compound. Further studies are needed to understand how this compound interacts with specific targets in the body. Additionally, the safety and toxicity profile of this compound need to be further investigated to determine its potential as a therapeutic agent.