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7-fluoro-1H-benzo[d]imidazole-2-carbaldehyde
$475.00
CAS No.: 615568-96-2
Catalog No.: 192606
Purity: 95%
MF: C8H5FN2O
MW: 164.139
Storage: 2-8 degree Celsius
SMILES: FC1=CC=CC2=C1NC(=N2)C=O
Catalog No.: 192606
Purity: 95%
MF: C8H5FN2O
MW: 164.139
Storage: 2-8 degree Celsius
SMILES: FC1=CC=CC2=C1NC(=N2)C=O
7-fluoro-1H-benzo[d]imidazole-2-carbaldehyde; CAS No.: 615568-96-2; 7-fluoro-1H-benzo[d]imidazole-2-carbaldehyde. PROPERTIES: 7-fluoro-1H-benzo[d]imidazole-2-carbaldehyde is a white to off-white crystalline powder with a molecular weight of 198.18 g/mol. It has a melting point between 190-195 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: 7-fluoro-1H-benzo[d]imidazole-2-carbaldehyde is predominantly used in pharmaceutical synthesis as an intermediate for creating antidepressant medications. The fluoro substituent on the benzo[d]imidazole ring enhances binding affinity to specific receptors in the brain, as described in psychopharmacology literature. Additionally, it serves as a building block for creating certain antiviral agents where the aldehyde group participates in forming covalent bonds with viral enzymes, as reported in antiviral chemistry studies. In agrochemical applications, it is utilized as a precursor for creating herbicides that target plant hormone biosynthesis pathways, where the fluoro-substituted ring system mimics natural plant regulators, as detailed in agricultural chemistry publications. The compound also finds application in materials science as a monomer for creating fluorescent polymers, where the benzo[d]imidazole structure contributes to photoluminescent properties, as outlined in polymer chemistry research. Furthermore, it is employed in analytical chemistry as a chiral derivatization agent for separating enantiomers of pharmaceutical compounds, where the benzo[d]imidazole framework forms diastereomeric complexes with racemic mixtures, as described in separation science literature. Its reactivity 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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