N-Methoxy-N-methyl 5-borono-2-fluorobenzamide

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Reagent Code: #121550
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CAS Number 874290-69-4

science Other reagents with same CAS 874290-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227 g/mol
Formula C₉H₁₁BFNO₄
badge Registry Numbers
MDL Number MFCD08235106
thermostat Physical Properties
Melting Point 160-163 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Primarily utilized in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals. Its boronic acid group enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs). The presence of the fluorine atom enhances its reactivity and selectivity in these reactions, making it valuable for constructing fluorinated aromatic compounds, which are increasingly important in drug design due to their metabolic stability and bioavailability. Additionally, it can be employed in the synthesis of agrochemicals and advanced materials, where precise molecular architecture is required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,402.00
inventory 250mg
10-20 days ฿1,359.00

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N-Methoxy-N-methyl 5-borono-2-fluorobenzamide
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Primarily utilized in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals. Its boronic acid group enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs). The presence of the fluorine atom enhances its reactivity and selectivity in these reactions, making it valuable for

Primarily utilized in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals. Its boronic acid group enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in creating active pharmaceutical ingredients (APIs). The presence of the fluorine atom enhances its reactivity and selectivity in these reactions, making it valuable for constructing fluorinated aromatic compounds, which are increasingly important in drug design due to their metabolic stability and bioavailability. Additionally, it can be employed in the synthesis of agrochemicals and advanced materials, where precise molecular architecture is required.

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