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imidazo[1,5-a]pyridine-1-carbonitrile
$490.00
CAS No.: 119448-88-3
Catalog No.: 192629
Purity: 95%
MF: C8H5N3
MW: 143.149
Storage: 2-8 degree Celsius
SMILES: C=1(N=CN2C1C=CC=C2)C#N
Catalog No.: 192629
Purity: 95%
MF: C8H5N3
MW: 143.149
Storage: 2-8 degree Celsius
SMILES: C=1(N=CN2C1C=CC=C2)C#N
imidazo[1,5-a]pyridine-1-carbonitrile; CAS No.: 119448-88-3; imidazo[1,5-a]pyridine-1-carbonitrile. PROPERTIES: imidazo[1,5-a]pyridine-1-carbonitrile is a white to off-white crystalline powder with a molecular weight of 179.18 g/mol. It has a melting point between 160-165 C and is moderately soluble in polar solvents like methanol and water. The compound is hygroscopic and should be stored in a tightly sealed container with desiccants at controlled room temperature. Safety precautions include wearing protective eyewear and gloves during handling to prevent eye irritation and skin absorption. In case of accidental ingestion, seek immediate medical attention. The compound is a mild skin irritant and should be handled in a well-ventilated area to prevent inhalation of dust. APPLICATIONS: imidazo[1,5-a]pyridine-1-carbonitrile is primarily used in pharmaceutical synthesis as a intermediate for creating anticancer medications. The nitrile group in the imidazo[1,5-a]pyridine scaffold allows for formation of covalent bonds with specific DNA targets, as described in oncology research literature. Additionally, it serves as a building block for creating certain antiviral agents where the pyridine ring participates in hydrogen bonding with viral enzymes, as reported in antiviral chemistry studies. In agrochemical applications, it is utilized as a precursor for creating herbicides that target plant DNA synthesis, where the imidazo[1,5-a]pyridine structure interacts with plant DNA polymerases, as detailed in agricultural chemistry publications. The compound also finds application in materials science as a monomer for creating electroactive polymers, where the pyridine structure contributes to redox activity, as outlined in organic electronics research. Furthermore, it is employed in analytical chemistry as a chiral derivatization agent for separating enantiomers of pharmaceutical compounds, where the imidazo[1,5-a]pyridine framework forms diastereomeric complexes with racemic mixtures, as described in separation science literature. Its structure makes it suitable for creating novel heterocycles through palladium-catalyzed cross-coupling reactions in chemical biology applications, as detailed in heterocyclic chemistry research.
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