4-(4-Boc-1-piperazinylcarbonyl)benzeneboronic acid pinacol ester

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Reagent Code: #90422
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CAS Number 864754-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.31 g/mol
Formula C₂₂H₃₃BN₂O₅
badge Registry Numbers
MDL Number MFCD08706021
thermostat Physical Properties
Melting Point 150-160°C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it serves as a boronic ester reagent. Its structure, featuring a Boc-protected piperazine moiety, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The Boc group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic ester functionality enables efficient carbon-carbon bond formation, making it a key intermediate in the development of drug candidates and biologically active compounds. Its application is especially prominent in medicinal chemistry for constructing diverse molecular frameworks.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,032.00
4-(4-Boc-1-piperazinylcarbonyl)benzeneboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it serves as a boronic ester reagent. Its structure, featuring a Boc-protected piperazine moiety, makes it valuable in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The Boc group provides stability during reactions, allowing selective deprotection when needed. Additionally, its boronic ester functionality enables efficient carbon-carbon bond formation, making it a key intermediate in the development of drug candidates and biologically active compounds. Its application is especially prominent in medicinal chemistry for constructing diverse molecular frameworks.
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