8-Bromo-6-nitroquinoline

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Reagent Code: #145595
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CAS Number 120287-30-1

science Other reagents with same CAS 120287-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.05 g/mol
Formula C₉H₅BrN₂O₂
thermostat Physical Properties
Melting Point 164°C
Boiling Point 377.3±22.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial, antimicrobial, antiviral, and anticancer agents. Its structure, featuring bromo and nitro groups, allows for selective functionalization through reactions such as nucleophilic substitution or condensation with other compounds, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It also serves in research settings to develop novel bioactive compounds and fluorescent probes due to its electron-withdrawing substituents that influence photophysical properties. Additionally, it functions as a reagent in bromine group transfer reactions or as a ligand in transition metal complexes to facilitate catalytic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,840.00
inventory 250mg
10-20 days ฿3,010.00
inventory 1g
10-20 days ฿8,420.00
inventory 5g
10-20 days ฿42,070.00
inventory 25mg
10-20 days ฿760.00

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8-Bromo-6-nitroquinoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial, antimicrobial, antiviral, and anticancer agents. Its structure, featuring bromo and nitro groups, allows for selective functionalization through reactions such as nucleophilic substitution or condensation with other compounds, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It also serves in research settings to develop novel bioactive compounds

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial, antimicrobial, antiviral, and anticancer agents. Its structure, featuring bromo and nitro groups, allows for selective functionalization through reactions such as nucleophilic substitution or condensation with other compounds, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It also serves in research settings to develop novel bioactive compounds and fluorescent probes due to its electron-withdrawing substituents that influence photophysical properties. Additionally, it functions as a reagent in bromine group transfer reactions or as a ligand in transition metal complexes to facilitate catalytic processes.

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