CAS 64951-07-1
:ethyl imidazo[1,2-a]pyrimidine-3-carboxylate
Description:
Ethyl imidazo[1,2-a]pyrimidine-3-carboxylate is a heterocyclic compound characterized by its imidazo and pyrimidine ring structures, which contribute to its unique chemical properties. This compound features an ethyl ester functional group, enhancing its solubility in organic solvents and influencing its reactivity. The presence of the carboxylate group allows for potential interactions in biological systems, making it of interest in medicinal chemistry. Ethyl imidazo[1,2-a]pyrimidine-3-carboxylate may exhibit various biological activities, including antimicrobial or anticancer properties, due to its structural similarity to nucleobases and other biologically relevant molecules. Its molecular structure can facilitate hydrogen bonding and π-π stacking interactions, which are crucial in drug design and development. Additionally, the compound's stability and reactivity can be influenced by substituents on the imidazo and pyrimidine rings, making it a versatile scaffold for further chemical modifications. Overall, this compound represents a significant class of heterocycles with potential applications in pharmaceuticals and agrochemicals.
Formula:C9H9N3O2
InChI:InChI=1/C9H9N3O2/c1-2-14-8(13)7-6-11-9-10-4-3-5-12(7)9/h3-6H,2H2,1H3
SMILES:CCOC(=O)c1cnc2ncccn12
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Found 4 products.
Ethyl imidazo[1,2-a]pyrimidine-3-carboxylate
CAS:Formula:C9H9N3O2Purity:97%Color and Shape:SolidMolecular weight:191.1867Ethyl imidazo[1,2-a]pyrimidine-3-carboxylate
CAS:<p>Ethyl imidazo[1,2-a]pyrimidine-3-carboxylate</p>Purity:95%Molecular weight:191.19g/molEthyl imidazo[1,2-a]pyrimidine-3-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H9N3O2Purity:Min. 95%Molecular weight:191.19 g/mol



