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Home  > 5-Amino-1-ethylpyridin-2(1H)-one

AV39847

1016710-71-6 | 5-Amino-1-ethylpyridin-2(1H)-one

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $254.00 $178.00 -   +
100mg 95% 1 week $354.00 $248.00 -   +
250mg 95% 1 week $485.00 $340.00 -   +
500mg 95% 1 week $772.00 $541.00 -   +
1g 95% 1 week $974.00 $682.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AV39847
Chemical Name: 5-Amino-1-ethylpyridin-2(1H)-one
CAS Number: 1016710-71-6
Molecular Formula: C7H10N2O
Molecular Weight: 138.1671
MDL Number: MFCD09815182
SMILES: CCn1cc(N)ccc1=O

 

Upstream Synthesis Route
  • 5-Amino-1-ethyl-1,2-dihydropyridin-2-one, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it particularly useful in the creation of heterocyclic compounds, which are key components in drug development and materials science.In chemical synthesis, $name$ can undergo various transformations to introduce functional groups, modify molecular structures, and generate new chemical entities. It can participate in a range of reactions, including nucleophilic substitution, condensation, and cyclization reactions, leading to the formation of diverse products with enhanced properties and biological activities. By leveraging the versatile nature of $name$, chemists can access a wide array of structurally complex molecules that are essential in drug discovery and materials design.Furthermore, the presence of the amino and carbonyl groups in 5-Amino-1-ethyl-1,2-dihydropyridin-2-one makes it a valuable intermediate for the synthesis of heterocyclic compounds such as pyridines, pyrroles, and pyrimidines. These heterocycles are prevalent in pharmaceuticals, agrochemicals, and functional materials due to their diverse biological activities and chemical reactivity. By incorporating $name$ into synthetic pathways, chemists can efficiently access these important heterocyclic frameworks, enabling the development of novel compounds with potential applications in various industries.
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