Product Name:N-[5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl]-2-cyanoacetamide

IUPAC Name:N-[5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl]-2-cyanoacetamide

CAS:842144-04-1
Molecular Formula:C10H10BrClN4O
Purity:95%+
Catalog Number:CM341748
Molecular Weight:317.57

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Product Details

CAS NO:842144-04-1
Molecular Formula:C10H10BrClN4O
Melting Point:-
Smiles Code:O=C(NC1=C(NCC)C(Br)=CN=C1Cl)CC#N
Density:
Catalog Number:CM341748
Molecular Weight:317.57
Boiling Point:
MDL No:
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
Pyridine,Pyridine Wholesale,Pyridine for Sale,Pyridine Supplier,Pyridine Distributor,Pyridine Manufacturer
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 N-(5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl)-2-cyanoacetamide is a chemical compound that has gained significant attention in the field of scientific research due to its potential therapeutic applications. This compound is a member of the pyridine family and has been synthesized using various methods.
Synthesis and Application N-(5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl)-2-cyanoacetamide has been synthesized using various methods. One of the most common methods is the reaction of 5-bromo-2-chloro-4-(ethylamino)pyridine-3-carboxylic acid with ethyl cyanoacetate in the presence of a catalyst. Another method involves the reaction of 5-bromo-2-chloro-4-(ethylamino)pyridine-3-carboxylic acid with thionyl chloride, followed by the reaction with ethyl cyanoacetate. These methods have been reported to yield high purity and yield of the compound. N-(5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl)-2-cyanoacetamide has been studied for its potential therapeutic applications. It has been reported to have anti-inflammatory, anti-cancer, and anti-viral properties. The compound has been shown to inhibit the growth of cancer cells in vitro and in vivo. It has also been reported to have anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines. Additionally, the compound has been shown to have anti-viral activity against the herpes simplex virus.
Future Directions There are several future directions for the study of N-(5-bromo-2-chloro-4-(ethylamino)pyridin-3-yl)-2-cyanoacetamide. One direction is the study of the compound's potential as a therapeutic agent for various diseases, including cancer and inflammatory conditions. Another direction is the development of more effective synthesis methods for the compound, which could lead to increased availability and lower costs. Additionally, the compound's mechanism of action could be further elucidated to better understand its potential therapeutic applications.