4-Methyl-3-(3-(4-methylpiperazin-1-yl)propoxy)phenylboronic acid

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Reagent Code: #90674
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CAS Number 1704064-31-2

science Other reagents with same CAS 1704064-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.19 g/mol
Formula C₁₅H₂₅BN₂O₃
badge Registry Numbers
MDL Number MFCD28384332
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. It is particularly valuable in the development of kinase inhibitors, which are crucial for targeted cancer therapies. Additionally, its piperazine moiety enhances solubility and bioavailability, making it a preferred choice in drug design. The compound's unique structure also allows for modifications to optimize pharmacokinetic properties, aiding in the creation of more effective and selective therapeutic agents.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,692.00

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4-Methyl-3-(3-(4-methylpiperazin-1-yl)propoxy)phenylboronic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. It is particularly valuable in the development of kinase inhibitors, which are crucial for targeted cancer therapies. Additionally, its piperazine moiety enhances solubility and bioavailability, making it a pre

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. It is particularly valuable in the development of kinase inhibitors, which are crucial for targeted cancer therapies. Additionally, its piperazine moiety enhances solubility and bioavailability, making it a preferred choice in drug design. The compound's unique structure also allows for modifications to optimize pharmacokinetic properties, aiding in the creation of more effective and selective therapeutic agents.

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