2,6-Dichloro-1,5-naphthyridine

95%

Reagent Code: #177598
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CAS Number 27017-66-9

science Other reagents with same CAS 27017-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.04 g/mol
Formula C₈H₄Cl₂N₂
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MDL Number MFCD03931483
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its rigid aromatic framework and electron-deficient nature. Commonly utilized in cross-coupling reactions to build complex molecules for drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,460.00
inventory 250mg
10-20 days ฿2,590.00
inventory 1g
10-20 days ฿7,680.00
inventory 5g
10-20 days ฿36,290.00

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2,6-Dichloro-1,5-naphthyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its rigid aromatic framework and electron-deficient nature. Commonly utilized in cross-coupling reactions to bui

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure enables selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to its rigid aromatic framework and electron-deficient nature. Commonly utilized in cross-coupling reactions to build complex molecules for drug discovery and materials science.

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