2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid

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Reagent Code: #62330
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CAS Number 680579-19-5

science Other reagents with same CAS 680579-19-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.31 g/mol
Formula C₁₂H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD03410260
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, particularly those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the piperazine moiety during synthetic processes, allowing for selective reactions to occur. Additionally, it serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the piperazine ring contributes to the desired pharmacological properties. Its application extends to research settings, where it is utilized in the study of biochemical pathways and the development of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,205.00
inventory 250mg
10-20 days ฿3,645.00
inventory 1g
10-20 days ฿8,100.00

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2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid
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This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, particularly those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the piperazine moiety during synthetic processes, allowing for selective reactions to occur. Additionally, it serves as an intermediate

This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, particularly those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the piperazine moiety during synthetic processes, allowing for selective reactions to occur. Additionally, it serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the piperazine ring contributes to the desired pharmacological properties. Its application extends to research settings, where it is utilized in the study of biochemical pathways and the development of novel therapeutic agents.

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