1-(4-Azidopiperidin-1-yl)ethan-1-one

95%

Reagent Code: #123820
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CAS Number 2098012-37-2

science Other reagents with same CAS 2098012-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.2 g/mol
Formula C₇H₁₂N₄O
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description Product Description

1-(4-Azidopiperidin-1-yl)ethan-1-yl)ethan-1-one is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. The azido group in its structure makes it valuable for click chemistry reactions, enabling efficient and selective coupling with alkynes to form triazole derivatives. This property is widely exploited in drug discovery and material science for creating complex molecular architectures. Additionally, it is employed in the preparation of piperidine-based compounds, which are commonly found in drugs targeting neurological disorders, inflammation, and other medical conditions. Its role in facilitating the construction of diverse chemical libraries underscores its importance in medicinal chemistry and chemical biology.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿20,313.00
250mg
10-20 days ฿52,830.00
1-(4-Azidopiperidin-1-yl)ethan-1-one
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1-(4-Azidopiperidin-1-yl)ethan-1-yl)ethan-1-one is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. The azido group in its structure makes it valuable for click chemistry reactions, enabling efficient and selective coupling with alkynes to form triazole derivatives. This property is widely exploited in drug discovery and

1-(4-Azidopiperidin-1-yl)ethan-1-yl)ethan-1-one is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. The azido group in its structure makes it valuable for click chemistry reactions, enabling efficient and selective coupling with alkynes to form triazole derivatives. This property is widely exploited in drug discovery and material science for creating complex molecular architectures. Additionally, it is employed in the preparation of piperidine-based compounds, which are commonly found in drugs targeting neurological disorders, inflammation, and other medical conditions. Its role in facilitating the construction of diverse chemical libraries underscores its importance in medicinal chemistry and chemical biology.

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