(5-Fluoro-2-((4-methylpiperazin-1-yl)methyl)phenyl)boronic acid hydrochloride

98%

Reagent Code: #90880
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CAS Number 1704065-33-7

science Other reagents with same CAS 1704065-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.56 g/mol
Formula C₁₂H₁₉BClFN₂O₂
badge Registry Numbers
MDL Number MFCD28400225
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for creating carbon-carbon bonds in the synthesis of complex organic compounds, including potential pharmaceuticals. The presence of the piperazine moiety enhances its potential for interaction with biological targets, often improving the pharmacokinetic properties of the resulting drug candidates. Researchers also explore its use in the development of kinase inhibitors, which are crucial in treating diseases like cancer. Additionally, its structural features make it a candidate for designing compounds with improved solubility and bioavailability, essential for effective drug delivery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,060.00

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(5-Fluoro-2-((4-methylpiperazin-1-yl)methyl)phenyl)boronic acid hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for creating carbon-carbon bonds in the synthesis of complex organic compounds, including potential pharmaceuticals. The presence of the piperazine moiety enhances its potential for interaction with biological targets, often improving the pharmacokinetic properties of the resulting drug candidates. Researchers also explore its use in the development of kinase inhibitors, which are crucial in treating diseases like cancer. Additionally, its structural features make it a candidate for designing compounds with improved solubility and bioavailability, essential for effective drug delivery.
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