6-Bromo-4-Chloro-3-Nitroquinoline

≥97%

Reagent Code: #147089
fingerprint
CAS Number 723281-72-9

science Other reagents with same CAS 723281-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.5 g/mol
Formula C₉H₄BrClN₂O₂
badge Registry Numbers
MDL Number MFCD09909913
thermostat Physical Properties
Boiling Point 387.626ºC
inventory_2 Storage & Handling
Density 1.834g/cm3
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds and in the preparation of fluorescent probes for biochemical assays. Due to its halogen and nitro groups, it serves as a versatile substrate in cross-coupling reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds in drug discovery pipelines.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿3,810.00
inventory 5g
10-20 days ฿15,660.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-4-Chloro-3-Nitroquinoline
No image available

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds and in the preparation of fluorescent probes for biochemical assays. Due to its halogen and nitro groups, it serves as a versatile subst

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex quinoline-based molecules. It is also employed in research settings to develop novel bioactive compounds and in the preparation of fluorescent probes for biochemical assays. Due to its halogen and nitro groups, it serves as a versatile substrate in cross-coupling reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds in drug discovery pipelines.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...