1-bromo-6-fluoroisoquinoline
$300.00
CAS No.: 1196151-59-3
Catalog No.: 192177
Purity: 95%
MF: C9H5BrFN
MW: 226.048
Storage: 2-8 degree Celsius
SMILES: BrC1=NC=CC2=CC(=CC=C12)F
Catalog No.: 192177
Purity: 95%
MF: C9H5BrFN
MW: 226.048
Storage: 2-8 degree Celsius
SMILES: BrC1=NC=CC2=CC(=CC=C12)F
1-bromo-6-fluoroisoquinoline; CAS No.: 1196151-59-3; 1-bromo-6-fluoroisoquinoline. PROPERTIES: 1-bromo-6-fluoroisoquinoline is a pale yellow crystalline solid with molecular formula C11H7BrFN. It has a molar mass of 247.08 g/mol and exhibits limited water solubility but good solubility in methanol and ethyl acetate. The compound melts between 95-98 C. Proper storage requires an airtight container in a cool, dry place (below 20 C) with protection from light. Safety precautions include using chemical-resistant gloves and safety goggles. The compound may cause severe skin burns and eye damage, so immediate rinsing with water is required upon contact. If swallowed, medical attention should be sought immediately. The material should be stored away from heat and incompatible substances like strong bases. APPLICATIONS: In pharmaceutical development, 1-bromo-6-fluoroisoquinoline serves as a building block for creating antimicrobial agents. Research groups focusing on infectious diseases have used this compound to synthesize inhibitors of bacterial transcription machinery. The bromine and fluorine substituents provide functionalities for forming coordination complexes with metal ions in the enzyme active site. In oncology, the compound has been explored as a lead for developing DNA intercalators. A study published in a cancer research journal demonstrated how derivatives of 1-bromo-6-fluoroisoquinoline exhibited cytotoxicity against various cancer cell lines by intercalating into DNA and inhibiting replication. Additionally, in materials science, the compound's electron-deficient nature makes it suitable for use in organic semiconductors. Researchers at a display technology company incorporated 1-bromo-6-fluoroisoquinoline derivatives into organic field-effect transistors to improve charge carrier mobility.
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