Methyl 6-Fluoro-1H-Indazole-3-Carboxylate

≥98%

Reagent Code: #79916
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CAS Number 885279-26-5

science Other reagents with same CAS 885279-26-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.16 g/mol
Formula C₉H₇FN₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its indazole core structure is particularly valuable in the design of potential drug candidates, especially those targeting enzyme inhibition or receptor modulation. The presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a useful building block in medicinal chemistry. It is often employed in the preparation of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or central nervous system (CNS) agents. Additionally, its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives for biological screening and optimization.

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inventory 1g
10-20 days ฿13,370.00

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Methyl 6-Fluoro-1H-Indazole-3-Carboxylate
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This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its indazole core structure is particularly valuable in the design of potential drug candidates, especially those targeting enzyme inhibition or receptor modulation. The presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a useful building block in medicinal chemistry. It is often employed in t

This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its indazole core structure is particularly valuable in the design of potential drug candidates, especially those targeting enzyme inhibition or receptor modulation. The presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a useful building block in medicinal chemistry. It is often employed in the preparation of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or central nervous system (CNS) agents. Additionally, its ester functional group allows for further chemical modifications, enabling the creation of diverse derivatives for biological screening and optimization.

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