Imidazo[1,5-a]pyridine-1-carboxaldehyde is a heterocyclic organic compound characterized by its fused imidazole and pyridine 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 nucleophilic additions and condensation reactions. It typically appears as a solid or liquid, depending on the specific conditions, and is soluble in polar organic solvents. The presence of both nitrogen atoms in the ring structure enhances its potential for coordination with metal ions, making it of interest in coordination chemistry and materials science. Additionally, compounds of this type may exhibit biological activity, which can be explored for pharmaceutical applications. Its molecular structure allows for diverse functionalization, enabling the synthesis of derivatives with tailored properties for specific applications in research and industry. Overall, Imidazo[1,5-a]pyridine-1-carboxaldehyde is a versatile compound with significant implications in organic synthesis and medicinal chemistry.

Imidazo[1,5-a]pyridine-1-carboxaldehyde

56671-67-1: Imidazo[1,5-a]pyridine-1-carboxaldehyde, 1-Formylimidazo[1,5-a]pyridine

Imidazo[1,5-a]pyridine-1-carbaldehyde

Imidazo[1,5-a]pyridine-1-carbaldehyde is a compound that belongs to the class of imidazopyridines. It is an environmentally friendly and sustainable molecule that has been shown to be fluorescent in water. Imidazo[1,5-a]pyridine-1-carbaldehyde has been shown to have photophysical properties such as fluorescence emission and chemiluminescence at room temperature. This compound also has applications in biomolecular chemistry and multicomponent reactions.

CAS 56671-67-1: Imidazo[1,5-a]pyridine-1-carboxaldehyde

Imidazo[1,5-a]pyridine-1-carbaldehyde

Ref: 54-OR953792

Imidazo[1,5-a]pyridine-1-carbaldehyde

Ref: 10-F092424

Imidazo[1,5-a]pyridine-1-carbaldehyde

Ref: 3D-FI42263

Imidazo[1,5-a]pyridine-1-carboxaldehyde (9CI)

Ref: IN-DA00EARP