Product Name:4-Methyl-3-nitropyridine hydrochloride

IUPAC Name:4-methyl-3-nitropyridine hydrochloride

CAS:856835-53-5
Molecular Formula:C6H7ClN2O2
Purity:95%
Catalog Number:CM176095
Molecular Weight:174.58

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CM176095-25g in stock ŞǑȡ

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Product Details

CAS NO:856835-53-5
Molecular Formula:C6H7ClN2O2
Melting Point:-
Smiles Code:Cl.CC1=C(C=NC=C1)[N+]([O-])=O
Density:
Catalog Number:CM176095
Molecular Weight:174.58
Boiling Point:
MDL No:MFCD09909573
Storage:Store at room temperature.

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 4-Methyl-3-nitropyridine hydrochloride, also known as 4-MNP-HCl, is a heterocyclic organic compound used in a variety of scientific research applications. It is a colorless solid that can be synthesized in several different ways and is soluble in most organic solvents. This compound has been studied extensively in the laboratory and has been found to have a variety of biochemical and physiological effects.
Synthesis and Application 4-Methyl-3-nitropyridine hydrochloride can be synthesized in several different ways. One method involves the reaction of pyridine with nitroethane and then reduction of the resulting nitropyridine with zinc and hydrochloric acid. Another method involves the reaction of 4-chloro-3-nitropyridine with sodium hydroxide and then hydrolysis of the resulting 4-chloro-3-nitropyridine hydrochloride with hydrochloric acid. Finally, 4-Methyl-3-nitropyridine hydrochloride can also be synthesized from the reaction of 3-nitropyridine with methyl iodide and then hydrolysis of the resulting 4-methyl-3-nitropyridine iodide with hydrochloric acid. 4-Methyl-3-nitropyridine hydrochloride has been widely used in scientific research. It has been used as a reagent in a variety of chemical reactions, including the synthesis of other organic compounds. It has also been used as a probe in studies of protein-ligand interactions and as a substrate in studies of enzyme kinetics. In addition, 4-Methyl-3-nitropyridine hydrochloride has been used in studies of the structure and function of biological membranes and as a fluorescent indicator for studies of calcium homeostasis.
Future Directions Despite the extensive research that has been done on 4-Methyl-3-nitropyridine hydrochloride, there are still many unanswered questions and possible future directions for research. For example, further research could be done to better understand the mechanism of action of this compound and its effects on cellular processes. In addition, further research could be done to develop new methods of synthesis and to explore the potential therapeutic applications of this compound. Finally, further research could also be done to explore the potential toxicity of this compound and to develop methods of reducing its toxicity.