CAS 143982-40-5
:Imidazo[1,2-a]pyrimidine-2-carboxaldehyde
Description:
Imidazo[1,2-a]pyrimidine-2-carboxaldehyde is a heterocyclic organic compound characterized by its fused imidazole and pyrimidine rings, which contribute to its unique chemical properties. This compound features a carboxaldehyde functional group, making it reactive and capable of participating in various chemical reactions, such as condensation and nucleophilic addition. It typically exhibits moderate solubility in polar solvents due to the presence of the aldehyde group, while its aromatic structure may impart some degree of hydrophobicity. The compound is of interest in medicinal chemistry and material science, often investigated for its potential biological activities, including antimicrobial and anticancer properties. Its molecular structure allows for various substitutions, which can lead to derivatives with enhanced or altered properties. Additionally, the presence of nitrogen atoms in the ring systems can influence its electronic characteristics, making it a valuable scaffold in drug design and development. Overall, Imidazo[1,2-a]pyrimidine-2-carboxaldehyde is a versatile compound with significant implications in research and application.
Formula:C7H5N3O
InChI:InChI=1S/C7H5N3O/c11-5-6-4-10-3-1-2-8-7(10)9-6/h1-5H
InChI key:InChIKey=BJPFFMZIQGNKKA-UHFFFAOYSA-N
SMILES:C(=O)C=1N=C2N(C1)C=CC=N2
Synonyms:- Imidazo[1,2-a]pyrimidine-2-carboxaldehyde
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Found 4 products.
Imidazo[1,2-a]pyrimidine-2-carboxaldehyde (9CI)
CAS:Formula:C7H5N3OPurity:95%Color and Shape:SolidMolecular weight:147.1341Imidazo[1,2-a]pyrimidine-2-carbaldehyde
CAS:<p>Imidazo[1,2-a]pyrimidine-2-carbaldehyde</p>Purity:95%Molecular weight:147.13g/molImidazo[1,2-a]pyrimidine-2-carbaldehyde
CAS:<p>Imidazo[1,2-a]pyrimidine-2-carboxaldehyde is a biologically active compound that is synthesized through a multicomponent reaction. The synthesis of imidazo[1,2-a]pyrimidine-2-carboxaldehyde requires sodium carbonate and malononitrile as starting materials. The reactants are activated with enolizable reagents such as pyran or acetone before being subjected to the reaction. This process yields target compounds with high yields and excellent spectroscopic properties.</p>Formula:C7H5N3OPurity:Min. 95%Molecular weight:147.14 g/mol



