1-(7-Bromoquinolin-3-yl)ethanone

98%

Reagent Code: #152373
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CAS Number 1228552-87-1

science Other reagents with same CAS 1228552-87-1

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scatter_plot Molecular Information
Weight 250.09 g/mol
Formula C₁₁H₈BrNO
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MDL Number MFCD22571333
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo-functionalized quinoline core allows for further cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when incorporated into larger molecular frameworks. Also utilized in the preparation of fluorescent probes and dyes, leveraging the inherent photophysical properties of the quinoline ring system for imaging and sensing applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,430.00
inventory 250mg
10-20 days ฿32,610.00
inventory 1g
10-20 days ฿91,880.00

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1-(7-Bromoquinolin-3-yl)ethanone
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo-functionalized quinoline core allows for further cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when incorporated into larger molecular frameworks. Also utilize

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo-functionalized quinoline core allows for further cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate biological activity when incorporated into larger molecular frameworks. Also utilized in the preparation of fluorescent probes and dyes, leveraging the inherent photophysical properties of the quinoline ring system for imaging and sensing applications.

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