4-(4-Ethylpiperazin-1-yl)phenylboronic acid pinacol ester

≥95%

Reagent Code: #183644
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CAS Number 656257-45-3

science Other reagents with same CAS 656257-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.25 g/mol
Formula C₁₈H₂₉BN₂O₂
badge Registry Numbers
MDL Number MFCD13190738
inventory_2 Storage & Handling
Density 1.1g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent to introduce arylboron functionality in the synthesis of pharmaceutical intermediates and bioactive molecules. Its piperazine-containing structure enhances solubility and binding affinity, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Stable under standard handling conditions, it facilitates efficient coupling with aryl halides in the construction of biaryl scaffolds found in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿980.00
inventory 1g
10-20 days ฿3,900.00
inventory 5g
10-20 days ฿18,540.00
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4-(4-Ethylpiperazin-1-yl)phenylboronic acid pinacol ester
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Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent to introduce arylboron functionality in the synthesis of pharmaceutical intermediates and bioactive molecules. Its piperazine-containing structure enhances solubility and binding affinity, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Stable under standard handling conditions, it facilitates efficient coupling with aryl halides in the construction of biaryl scaffolds found in d

Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent to introduce arylboron functionality in the synthesis of pharmaceutical intermediates and bioactive molecules. Its piperazine-containing structure enhances solubility and binding affinity, making it valuable in medicinal chemistry for developing kinase inhibitors and receptor modulators. Stable under standard handling conditions, it facilitates efficient coupling with aryl halides in the construction of biaryl scaffolds found in drug discovery programs.

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