5-Bromoquinolin-8-amine

97%

Reagent Code: #148119
label
Alias 3H-[1,2,3]triazolo[4,5-D]pyrimidin-7-ol; 5-bromo-8-quinolineamine; 5-bromo-8-aminoquinoline
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CAS Number 53472-18-7

science Other reagents with same CAS 53472-18-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.07 g/mol
Formula C₉H₇BrN₂
badge Registry Numbers
MDL Number MFCD01571832
thermostat Physical Properties
Melting Point 109-110 °C
Boiling Point 353.3°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.649±0.06 g/cm3(Predicted)
Storage 2-8℃, inert gas, avoiding light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of complex heterocyclic compounds that interact with biological targets such as kinases and DNA. Also employed in research for developing fluorescent probes due to its ability to form stable complexes with metals and exhibit luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving quinoline-based drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿420.00
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿4,280.00
inventory 10g
10-20 days ฿8,290.00
inventory 25g
10-20 days ฿17,440.00

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5-Bromoquinolin-8-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of complex heterocyclic compounds that interact with biological targets such as kinases and DNA. Also employed in research for developing fluorescent probes due to its ability to form stable complexes with metals and exhibit luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of complex heterocyclic compounds that interact with biological targets such as kinases and DNA. Also employed in research for developing fluorescent probes due to its ability to form stable complexes with metals and exhibit luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving quinoline-based drug candidates.
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