4-Fluoro-1-isopropyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazole

≥95%

Reagent Code: #118900
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CAS Number 1231930-37-2

science Other reagents with same CAS 1231930-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.19 g/mol
Formula C₁₇H₂₄BFN₂O₂
badge Registry Numbers
MDL Number MFCD25977327
thermostat Physical Properties
Boiling Point 442.7±30.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it may be used in material science for creating advanced polymers or organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice in various chemical transformations.

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Test Parameter Specification
Appearance Light Gray Powder
Purity (%) 95-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿14,445.00
inventory 100mg
10-20 days ฿1,296.00
inventory 250mg
10-20 days ฿1,944.00
inventory 1g
10-20 days ฿4,806.00

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4-Fluoro-1-isopropyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazole
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it may be used in material science for creating advanced polymers or organic electronic materials. Its stability and reactivity under mild conditions make it a preferred choice in various chemical transformations.
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