3-Fluoro-4-((4-methylpiperazin-1-yl)methyl)phenylboronic acid

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Reagent Code: #90142
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CAS Number 1334401-01-2

science Other reagents with same CAS 1334401-01-2

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scatter_plot Molecular Information
Weight 252.1 g/mol
Formula C₁₂H₁₈BFN₂O₂
badge Registry Numbers
MDL Number MFCD16198075
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of pharmaceuticals and complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it useful in constructing biologically active compounds. Additionally, the presence of the piperazine moiety enhances its potential for interaction with biological targets, particularly in the design of drug candidates targeting CNS disorders or cancer. Its fluorine atom further improves metabolic stability and binding affinity, making it a versatile building block in drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿31,350.00
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3-Fluoro-4-((4-methylpiperazin-1-yl)methyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of pharmaceuticals and complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it useful in constructing biologically active compounds. Additionally, the presence of the piperazine moiety enhances its pot

This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of pharmaceuticals and complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it useful in constructing biologically active compounds. Additionally, the presence of the piperazine moiety enhances its potential for interaction with biological targets, particularly in the design of drug candidates targeting CNS disorders or cancer. Its fluorine atom further improves metabolic stability and binding affinity, making it a versatile building block in drug discovery.

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