Product Name:Ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate

IUPAC Name:ethyl 2-(2-chloro-4-formylphenoxy)pyridine-4-carboxylate

CAS:1415719-37-7
Molecular Formula:C15H12ClNO4
Purity:97%
Catalog Number:CM503079
Molecular Weight:305.71

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CM503079-1g in stock ƩǠȋ

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Product Details

CAS NO:1415719-37-7
Molecular Formula:C15H12ClNO4
Melting Point:-
Smiles Code:O=C(OCC)C1=CC=NC(OC2=CC=C(C=O)C=C2Cl)=C1
Density:
Catalog Number:CM503079
Molecular Weight:305.71
Boiling Point:
MDL No:MFCD22689500
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.


Product Other Information

Product Overview Ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate, also known as ECPI, is a chemical compound that has been used in a variety of scientific research applications. It is an organic compound that has a unique structure, with a phenoxy group connected to a chloro-formyl group. This compound is used in a variety of ways in laboratory experiments, and it has been found to have a number of biochemical and physiological effects.
Synthesis and Application Ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate can be synthesized through a three-step process. First, 2-chloro-4-formylphenoxyacetic acid is reacted with ethyl isonicotinate in the presence of an acid catalyst. This reaction produces the ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate. The second step involves the hydrolysis of the reaction product in the presence of a base catalyst. This reaction produces the ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate. Finally, the compound is purified by recrystallization. Ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate has been used in a variety of scientific research applications. It has been used in the study of enzyme inhibition, protein-protein interactions, and signal transduction. It has also been used in the study of the effects of drugs on cell proliferation and apoptosis.
Future Directions There are a number of potential future directions for the use of Ethyl 2-(2-chloro-4-formylphenoxy)isonicotinate in scientific research. It could be used to study the effects of environmental pollutants on the body, as well as the effects of drugs on cell proliferation and apoptosis. Additionally, it could be used to study the effects of drugs on the immune system, as well as the metabolism of lipids and carbohydrates. Furthermore, it could be used to study the effects of enzyme inhibition, protein-protein interactions, and signal transduction. Finally, it could be used to study the effects of drugs on the brain, as well as the effects of drugs on behavior.