Ethyl 6-bromo-4-fluoro-1H-indole-2-carboxylate

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Reagent Code: #49918
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CAS Number 396075-55-1

science Other reagents with same CAS 396075-55-1

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Weight 286.0900 g/mol
Formula C₁₁H₉NO₂FBr
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Ethyl 6-bromo-4-fluoro-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromo and fluoro substituents on the indole ring, makes it a valuable building block in medicinal chemistry. Researchers often utilize it to synthesize potential drug candidates, particularly in the exploration of compounds with biological activity, such as anticancer, antiviral, or anti-inflammatory agents. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse indole derivatives for pharmacological studies and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,564.00

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Ethyl 6-bromo-4-fluoro-1H-indole-2-carboxylate
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Ethyl 6-bromo-4-fluoro-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromo and fluoro substituents on the indole ring, makes it a valuable building block in medicinal chemistry. Researchers often utilize it to synthesize potential drug candidates, particularly in the exploration of compounds with biological activity, such as anticancer, antiviral, or anti-inflammatory agents. Additionally,

Ethyl 6-bromo-4-fluoro-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromo and fluoro substituents on the indole ring, makes it a valuable building block in medicinal chemistry. Researchers often utilize it to synthesize potential drug candidates, particularly in the exploration of compounds with biological activity, such as anticancer, antiviral, or anti-inflammatory agents. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse indole derivatives for pharmacological studies and drug discovery.

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