(4-(1-(4-Methylpiperazin-1-yl)ethyl)phenyl)boronic acid hydrochloride

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Reagent Code: #91231
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CAS Number 1704069-16-8

science Other reagents with same CAS 1704069-16-8

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scatter_plot Molecular Information
Weight 284.6 g/mol
Formula C₁₃H₂₂BClN₂O₂
badge Registry Numbers
MDL Number MFCD28384341
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its boronic acid group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex organic frameworks. The 4-methylpiperazine moiety enhances its solubility and binding affinity, making it useful in designing drug candidates targeting specific enzymes or receptors. It is also employed in the preparation of proteasome inhibitors and other therapeutic agents, contributing to advancements in medicinal chemistry.

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inventory 1g
10-20 days ฿38,169.00

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(4-(1-(4-Methylpiperazin-1-yl)ethyl)phenyl)boronic acid hydrochloride
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its boronic acid group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex organic frameworks. The 4-methylpiperazine moiety enhances its solubility and binding affinity, making it useful in designing drug candidates targeting specific enzymes or rec

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of biologically active molecules. Its boronic acid group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex organic frameworks. The 4-methylpiperazine moiety enhances its solubility and binding affinity, making it useful in designing drug candidates targeting specific enzymes or receptors. It is also employed in the preparation of proteasome inhibitors and other therapeutic agents, contributing to advancements in medicinal chemistry.

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