Product Name:2-(4-Fluorobenzoyl)-4-methylpyridine

IUPAC Name:2-(4-fluorobenzoyl)-4-methylpyridine

CAS:497854-55-4
Molecular Formula:C13H10FNO
Purity:95%+
Catalog Number:CM579976
Molecular Weight:215.23

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Product Details

CAS NO:497854-55-4
Molecular Formula:C13H10FNO
Melting Point:-
Smiles Code:CC1=CC(=NC=C1)C(=O)C1=CC=C(F)C=C1
Density:
Catalog Number:CM579976
Molecular Weight:215.23
Boiling Point:
MDL No:MFCD13152712
Storage:

Category Infos

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.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
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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-(4-Fluorobenzoyl)-4-methylpyridine is a chemical compound with the molecular formula C13H10FNO. It is a pyridine derivative that consists of a pyridine ring substituted at the 4-position with a methyl group and at the 2-position with a 4-fluorobenzoyl group.
The compound has a molecular weight of approximately 215.23 grams per mole. It appears as a yellow crystalline solid at room temperature.
2-(4-Fluorobenzoyl)-4-methylpyridine is often used as an intermediate in the synthesis of various pharmaceutical compounds and organic molecules. Its unique structure and functional groups make it a valuable building block for the development of new drugs and chemical compounds.
Synthesis and Application 2-(4-Fluorobenzoyl)-4-methylpyridine can be synthesized through a multi-step reaction. The first step involves reacting 4-fluorobenzaldehyde with 4-methylpyridine in a reaction catalyzed by p-toluenesulfonic acid. This reaction yields 2-(4-fluorobenzoyl)-4-methylpyridine. The second step involves reacting the resulting 2-(4-Fluorobenzoyl)-4-methylpyridine with acetic anhydride in a reaction catalyzed by p-toluenesulfonic acid. This reaction yields 2-(4-fluorobenzoyl)-4-methylpyridine acetate. 2-(4-Fluorobenzoyl)-4-methylpyridine has been used in a variety of scientific research applications. For example, it has been used in the synthesis of a variety of organic compounds, including quinolines and pyridines. It has also been used in the synthesis of biologically active compounds, such as drugs and natural products. In addition, 2-(4-Fluorobenzoyl)-4-methylpyridine has been used in biochemical and physiological research, such as the study of enzyme kinetics, cell signaling pathways, and drug metabolism.
Future Directions The use of 2-(4-Fluorobenzoyl)-4-methylpyridine in scientific research is a relatively new field, and there are many potential future directions for research. For example, further research could be conducted to better understand the mechanism of action of 2-(4-Fluorobenzoyl)-4-methylpyridine and its effects on biochemical and physiological processes. In addition, further research could be conducted to develop more efficient and cost-effective methods for synthesizing 2-(4-Fluorobenzoyl)-4-methylpyridine. Finally, further research could be conducted to explore the potential applications of 2-(4-Fluorobenzoyl)-4-methylpyridine in drug development and other areas of medicine.