2,4-Dibromo-1,8-naphthyridine

97%

Reagent Code: #130680
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CAS Number 54569-27-6

science Other reagents with same CAS 54569-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.94 g/mol
Formula C₈H₄Br₂N₂
badge Registry Numbers
MDL Number MFCD14705080
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its rigid aromatic framework and electron-deficient character. Commonly utilized in cross-coupling reactions such as Suzuki and Heck reactions to build complex molecules for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,770.00
inventory 250mg
10-20 days ฿9,800.00
inventory 1g
10-20 days ฿26,440.00
2,4-Dibromo-1,8-naphthyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its rigid aromatic framework and electron-deficient character. Commonly utilized in cross-coupling reactions such as

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and anticancer agents. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Also employed in materials science for designing organic semiconductors and fluorescent dyes due to its rigid aromatic framework and electron-deficient character. Commonly utilized in cross-coupling reactions such as Suzuki and Heck reactions to build complex molecules for research and industrial applications.

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