4-(3-(4-Methylpiperazin-1-yl)propoxy)phenylboronic acid

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Reagent Code: #90376
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CAS Number 1003028-43-0

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scatter_plot Molecular Information
Weight 278.16 g/mol
Formula C₁₄H₂₃BN₂O₃
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MDL Number MFCD22418297
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its structure, featuring a methylpiperazine moiety, suggests potential applications in drug development, particularly in designing compounds with enhanced bioavailability or targeting specific biological pathways. Its boronic acid group also allows for interactions with biological molecules, making it a candidate for use in biochemical assays or as a building block in the development of enzyme inhibitors or receptor modulators.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days $1,150.35
4-(3-(4-Methylpiperazin-1-yl)propoxy)phenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which is pivotal in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its structure, featuring a methylpiperazine moiety, suggests potential applications in drug development, particularly in designing compounds with enhanced bioavailability or targeting specific biological pathways. Its boronic acid group also allows for interactions with biological molecules, making it a candidate for use in biochemical assays or as a building block in the development of enzyme inhibitors or receptor modulators.
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