tert-Butyl 3-fluoro-4-((methylsulfonyloxy)methyl)piperidine-1-carboxylate

98%

Reagent Code: #124183
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CAS Number 1824168-69-5

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blur_circular Chemical Specifications

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Weight 311.37 g/mol
Formula C₁₂H₂₂FNO₅S
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description Product Description

This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring a piperidine ring and functional groups like fluoro and methylsulfonyloxy, makes it valuable for designing drugs targeting neurological disorders, pain management, and other therapeutic areas. The tert-butyl group enhances stability, facilitating easier handling during chemical reactions. It is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug candidates for improved efficacy and safety. Additionally, its reactivity allows for further modifications, making it a versatile building block in organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿50,040.00
inventory 100mg
10-20 days ฿24,948.00

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tert-Butyl 3-fluoro-4-((methylsulfonyloxy)methyl)piperidine-1-carboxylate
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This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring a piperidine ring and functional groups like fluoro and methylsulfonyloxy, makes it valuable for designing drugs targeting neurological disorders, pain management, and other therapeutic areas. The tert-butyl group enhances stability, facilitating easier handling during chemical reactions. It is often employed in medicinal chemistry to explo

This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring a piperidine ring and functional groups like fluoro and methylsulfonyloxy, makes it valuable for designing drugs targeting neurological disorders, pain management, and other therapeutic areas. The tert-butyl group enhances stability, facilitating easier handling during chemical reactions. It is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug candidates for improved efficacy and safety. Additionally, its reactivity allows for further modifications, making it a versatile building block in organic synthesis.

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