4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

97%

Reagent Code: #118916
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CAS Number 1152441-29-6

science Other reagents with same CAS 1152441-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.08 g/mol
Formula C₁₂H₁₇BFNO₂
badge Registry Numbers
MDL Number MFCD16996293
thermostat Physical Properties
Boiling Point 356.4±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its fluorine substituent enhances its utility in the design of molecules with improved metabolic stability and binding affinity. Researchers often employ it in the development of novel materials and ligands for catalytic processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,436.00
inventory 5g
10-20 days ฿23,949.00
inventory 250mg
10-20 days ฿2,133.00
inventory 100mg
10-20 days ฿1,404.00

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4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its fluorine substituent enhance

This chemical is primarily used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its fluorine substituent enhances its utility in the design of molecules with improved metabolic stability and binding affinity. Researchers often employ it in the development of novel materials and ligands for catalytic processes.

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