Potassium trifluoro(3-((4-nitrophenyl)amino)-3-oxopropyl)borate

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Reagent Code: #91074
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CAS Number 1705578-36-4

science Other reagents with same CAS 1705578-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.09 g/mol
Formula C₉H₉BF₃KN₂O₃
badge Registry Numbers
MDL Number MFCD28805730
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis as a reagent for the formation of carbon-boron bonds, which are crucial in various cross-coupling reactions. It facilitates the introduction of trifluoroborate groups into organic molecules, enhancing their reactivity and stability. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it aids in the creation of bioactive compounds. Its role in Suzuki-Miyaura cross-coupling reactions is notable, as it helps in constructing carbon-carbon bonds efficiently, which is essential for producing diverse organic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,200.00
inventory 250mg
10-20 days ฿32,400.00
inventory 1g
10-20 days ฿84,240.00

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Potassium trifluoro(3-((4-nitrophenyl)amino)-3-oxopropyl)borate
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This chemical is primarily used in organic synthesis as a reagent for the formation of carbon-boron bonds, which are crucial in various cross-coupling reactions. It facilitates the introduction of trifluoroborate groups into organic molecules, enhancing their reactivity and stability. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it aids in

This chemical is primarily used in organic synthesis as a reagent for the formation of carbon-boron bonds, which are crucial in various cross-coupling reactions. It facilitates the introduction of trifluoroborate groups into organic molecules, enhancing their reactivity and stability. This makes it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of complex molecules, particularly in medicinal chemistry, where it aids in the creation of bioactive compounds. Its role in Suzuki-Miyaura cross-coupling reactions is notable, as it helps in constructing carbon-carbon bonds efficiently, which is essential for producing diverse organic compounds.

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