(4-((4-(tert-Butoxycarbonyl)piperazin-1-yl)sulfonyl)-3,5-dimethylphenyl)boronic acid

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Reagent Code: #89194
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CAS Number 1704069-12-4

science Other reagents with same CAS 1704069-12-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.29 g/mol
Formula C₁₇H₂₇BN₂O₆S
badge Registry Numbers
MDL Number MFCD28384280
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the formation of carbon-carbon bonds. Its piperazine and tert-butoxycarbonyl (Boc) groups make it a valuable intermediate in the development of pharmaceuticals, especially in the synthesis of complex molecules like kinase inhibitors or other biologically active compounds. The Boc group provides protection for the piperazine nitrogen during synthetic processes, allowing for selective reactions. Additionally, its sulfonyl group enhances the compound's reactivity and stability, making it suitable for use in medicinal chemistry research and drug discovery.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,950.00
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(4-((4-(tert-Butoxycarbonyl)piperazin-1-yl)sulfonyl)-3,5-dimethylphenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the formation of carbon-carbon bonds. Its piperazine and tert-butoxycarbonyl (Boc) groups make it a valuable intermediate in the development of pharmaceuticals, especially in the synthesis of complex molecules like kinase inhibitors or other biologically active compounds. The Boc group provides protection for the piperazine nitrogen during

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the formation of carbon-carbon bonds. Its piperazine and tert-butoxycarbonyl (Boc) groups make it a valuable intermediate in the development of pharmaceuticals, especially in the synthesis of complex molecules like kinase inhibitors or other biologically active compounds. The Boc group provides protection for the piperazine nitrogen during synthetic processes, allowing for selective reactions. Additionally, its sulfonyl group enhances the compound's reactivity and stability, making it suitable for use in medicinal chemistry research and drug discovery.

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