cas 13081-75-9|| where to buy Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate

Product Name:Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate

IUPAC Name:ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate

: CAS：13081-75-9; Molecular Formula：C9H13NO3; Purity：95%

: Catalog Number：CM172709; Molecular Weight：183.21

Packing Unit	Available Stock	Price($)	Quantity
CM172709-1g	1-2 Weeks	ŤƈƿŤ

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Product Details

: CAS NO:13081-75-9; Molecular Formula:C9H13NO3; Melting Point:-; Smiles Code:O=C(C1=C(C)NCCC1=O)OCC; Density:

: Catalog Number:CM172709; Molecular Weight:183.21; Boiling Point:; MDL No:MFCD20689879; 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	Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate, also known as EMTOC, is a synthetic molecule that has been used in a variety of scientific applications. It is a derivative of the pyridine ring, which is a nitrogen-containing heterocyclic compound. EMTOC has a wide range of uses, including in organic synthesis, as a drug delivery system, and as a catalyst in biochemical reactions.
Synthesis and Application	Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate can be synthesized using a variety of methods, including the Fischer indole synthesis and the Knoevenagel condensation. The Fischer indole synthesis involves the reaction of an aldehyde or ketone with an amine to form a pyridine. The Knoevenagel condensation is a reaction between an aldehyde or ketone and a secondary amine to form a beta-keto-ester. Both of these methods can be used to synthesize Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate from the appropriate starting materials. Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate has been used in a variety of scientific applications, including as a drug delivery system, as a catalyst in biochemical reactions, and as a reagent in organic synthesis. It has also been used as an inhibitor of the enzyme acetylcholinesterase, which is involved in the breakdown of the neurotransmitter acetylcholine. In addition, Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate has been used as a substrate for the enzyme tyrosinase, which is involved in the biosynthesis of melanin. Furthermore, Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate has been used as a ligand in the study of metal-ion complexes.
Future Directions	There are a number of potential future directions for research into the use of Ethyl 2-methyl-4-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate. For example, further research could be conducted into its mechanism of action, which would allow for a better understanding of its effects. In addition, further research could be conducted into its use as a drug delivery system, which could lead to new and improved treatments for a variety of conditions. Furthermore, research could be conducted into its potential use as an inhibitor or activator of other enzymes, which could lead to new and improved treatments for a variety of diseases. Finally, research could be conducted into its potential use as a catalyst in biochemical reactions, which could lead to new and improved methods for synthesizing a variety of compounds.