Methyl 7-fluoro-1H-indole-6-carboxylate

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Reagent Code: #50180
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CAS Number 1427366-38-8

science Other reagents with same CAS 1427366-38-8

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Weight 193.17 g/mol
Formula C₁₀H₈FNO₂
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MDL Number MFCD23706323
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a fluoro group, an indole moiety, and a carboxylate ester group, makes it a valuable intermediate for creating molecules with potential biological activity. It is often employed in the design of compounds targeting neurological disorders, cancer, and inflammation due to its ability to interact with specific enzymes and receptors. Additionally, it serves as a building block in organic synthesis, enabling the construction of complex heterocyclic frameworks that are essential in medicinal chemistry. Its applications extend to the development of fluorescent probes and imaging agents, leveraging its indole core for optical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,154.00

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Methyl 7-fluoro-1H-indole-6-carboxylate
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a fluoro group, an indole moiety, and a carboxylate ester group, makes it a valuable intermediate for creating molecules with potential biological activity. It is often employed in the design of compounds targeting neurological disorders, cancer, and inflammation due to its ability to interact with specific enzymes and receptors. Additionally, it

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a fluoro group, an indole moiety, and a carboxylate ester group, makes it a valuable intermediate for creating molecules with potential biological activity. It is often employed in the design of compounds targeting neurological disorders, cancer, and inflammation due to its ability to interact with specific enzymes and receptors. Additionally, it serves as a building block in organic synthesis, enabling the construction of complex heterocyclic frameworks that are essential in medicinal chemistry. Its applications extend to the development of fluorescent probes and imaging agents, leveraging its indole core for optical properties.

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