4-((4-(tert-Butoxycarbonyl)piperazin-1-yl)methyl)-3-fluorophenylboronic acid

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Reagent Code: #90311
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CAS Number 1704064-00-5

science Other reagents with same CAS 1704064-00-5

blur_circular Chemical Specifications

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Weight 338.19 g/mol
Formula C₁₆H₂₄BFN₂O₄
badge Registry Numbers
MDL Number MFCD28384232
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperazine group, makes it valuable in medicinal chemistry for constructing complex molecules, especially in the development of pharmaceuticals. The fluorine atom enhances its reactivity and selectivity in certain transformations. Additionally, it serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and functional groups make it a versatile building block in chemical research and drug discovery.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,860.00

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4-((4-(tert-Butoxycarbonyl)piperazin-1-yl)methyl)-3-fluorophenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperazine group, makes it valuable in medicinal chemistry for constructing complex molecules, especially in the development of pharmaceuticals. The fluorine atom enhances its reactivity and selectivity in certain transformations. Additionally, it serves as an intermediate in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and functional groups make it a versatile building block in chemical research and drug discovery.
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