6-Bromo-4-hydroxy-3-nitroquinoline

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Reagent Code: #143636
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CAS Number 853908-50-6

science Other reagents with same CAS 853908-50-6

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Weight 269.05 g/mol
Formula C₉H₅BrN₂O₃
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MDL Number MFCD09800413
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in research settings to develop fluorescent probes due to the inherent photophysical properties of the quinoline scaffold. The bromo and nitro groups serve as reactive sites for cross-coupling and reduction reactions, enabling the construction of complex heterocyclic systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿132.00
inventory 1g
10-20 days ฿154.00
inventory 25g
10-20 days ฿5,440.00
inventory 5g
10-20 days ฿1,100.00

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6-Bromo-4-hydroxy-3-nitroquinoline
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Used as an intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in research settings to develop fluorescent probes due to the inherent photophysical properties of the quinoline scaffold. The bromo and nitro groups serve as reactive sites for cross-coupling and reduction reactions, e
Used as an intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure allows for further functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in research settings to develop fluorescent probes due to the inherent photophysical properties of the quinoline scaffold. The bromo and nitro groups serve as reactive sites for cross-coupling and reduction reactions, enabling the construction of complex heterocyclic systems.
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