Ethyl 5-bromo-1, 7-naphthyridine-3-carboxylate

98%

Reagent Code: #184863
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CAS Number 1646882-61-2

science Other reagents with same CAS 1646882-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.11 g/mol
Formula C₁₁H₉BrN₂O₂
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with potential biological activity. Also utilized in research settings to develop fluorescent probes due to the inherent photophysical properties of the naphthyridine core.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,980.00
inventory 100mg
10-20 days ฿15,200.00
inventory 250mg
10-20 days ฿22,800.00

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Ethyl 5-bromo-1, 7-naphthyridine-3-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with potential biological activity. Also utilized in research settin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for creating libraries of compounds in drug discovery. Commonly employed in cross-coupling reactions to introduce aryl or heteroaryl groups, enabling the construction of complex molecules with potential biological activity. Also utilized in research settings to develop fluorescent probes due to the inherent photophysical properties of the naphthyridine core.

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