Product Name:Methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate

IUPAC Name:methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate

CAS:1457612-06-4
Molecular Formula:C12H15FN2O2
Purity:95%+
Catalog Number:CM472785
Molecular Weight:238.26

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CM472785-100mg 1-2 Weeks ǟŁ
CM472785-250mg 3-4 Weeks Ĝřţ
CM472785-1g 3-4 Weeks ƏǭƏ
CM472785-5g 4-5 Weeks ǟţŽ

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Product Details

CAS NO:1457612-06-4
Molecular Formula:C12H15FN2O2
Melting Point:-
Smiles Code:COC(=O)C1CCN(CC1)C1=NC=C(F)C=C1
Density:
Catalog Number:CM472785
Molecular Weight:238.26
Boiling Point:
MDL No:MFCD15508171
Storage:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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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.
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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 Methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate, also known as Methyl 5-Fluoro-2-Pyridyl-4-Piperidinylcarboxylate, is a chemical compound that has been synthesized and studied for its potential applications in scientific research. This compound is of interest due to its unique chemical structure and potential for use as a tool in various research fields.
Synthesis and Application The synthesis of Methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate involves a multi-step process that requires specialized knowledge and equipment. One common method for synthesizing this compound involves the reaction of 5-fluoropyridine-2-carboxylic acid with piperidine-4-carboxylic acid in the presence of a coupling reagent such as EDCI or DCC. The resulting intermediate is then treated with methyl iodide to yield the final product. Methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate has been used in a variety of scientific research applications. One area of interest is in the field of medicinal chemistry, where this compound has been studied for its potential as a drug lead for the treatment of various diseases. It has also been used as a tool in neuroscience research, where it has been shown to modulate the activity of certain neurotransmitter receptors.
Future Directions There are many potential future directions for the study of Methyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate. One area of interest is in the development of more potent analogs of this compound that could be used as drug leads for the treatment of various diseases. Another area of interest is in the further characterization of the mechanism of action of this compound, which could provide insight into the function of certain neurotransmitter receptors and their role in disease states. Additionally, this compound could be used as a tool in the study of neural circuits and behavior, as its effects on neurotransmitter release and synaptic transmission could be used to probe the underlying mechanisms of these processes.