ethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)oxazole-4-carboxylate

Reagent Code: #50393
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CAS Number 1037797-93-5

science Other reagents with same CAS 1037797-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.37 g/mol
Formula C₁₆H₂₄N₂O₅
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex chemical structures, often in the synthesis of piperidine-containing compounds, which are prevalent in many drugs. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthesis, allowing for precise modifications. Its oxazole moiety is valuable in medicinal chemistry, contributing to the development of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Overall, it plays a crucial role in the efficient and targeted synthesis of biologically active molecules.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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ethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)oxazole-4-carboxylate
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This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex chemical structures, often in the synthesis of piperidine-containing compounds, which are prevalent in many drugs. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthesis, allowing for precise modifications. Its oxazole moiety is valuable in medicinal chemistry, c

This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the construction of complex chemical structures, often in the synthesis of piperidine-containing compounds, which are prevalent in many drugs. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step synthesis, allowing for precise modifications. Its oxazole moiety is valuable in medicinal chemistry, contributing to the development of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Overall, it plays a crucial role in the efficient and targeted synthesis of biologically active molecules.

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