5-Iodoquinolin-8-amine

≥95%

Reagent Code: #200246
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CAS Number 142340-15-6

science Other reagents with same CAS 142340-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.07 g/mol
Formula C₉H₇IN₂
badge Registry Numbers
MDL Number MFCD24160460
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and reactive amine group. The iodo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecular structures. Also employed in materials science for designing fluorescent probes and sensors, leveraging its nitrogen-containing heterocyclic framework.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,520.00
inventory 1g
10-20 days ฿5,360.00
5-Iodoquinolin-8-amine
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and reactive amine group. The iodo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecular structures. Also employed in materials science for designing fluorescent probes and sensors, leveraging its nitroge

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Serves as a building block in the development of antimalarial and anticancer agents due to its quinoline core and reactive amine group. The iodo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecular structures. Also employed in materials science for designing fluorescent probes and sensors, leveraging its nitrogen-containing heterocyclic framework.

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