(4-(Cyclohexylcarbamoyl)-3-fluorophenyl)boronic acid

97%

Reagent Code: #90669
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CAS Number 874289-11-9

science Other reagents with same CAS 874289-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.09 g/mol
Formula C₁₃H₁₇BFNO₃
thermostat Physical Properties
Melting Point 157-159°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclohexyl and fluorine substituents enhance its stability and reactivity, allowing for selective and efficient coupling with various aryl halides. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the design of novel polymers and advanced materials.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,280.00
inventory 250mg
10-20 days ฿2,410.00

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(4-(Cyclohexylcarbamoyl)-3-fluorophenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclohexyl and fluorine substituents enhance its stability and reactivity, allowing for selective and efficient coupling with various aryl halides. Additionally, it is employed in the deve

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclohexyl and fluorine substituents enhance its stability and reactivity, allowing for selective and efficient coupling with various aryl halides. Additionally, it is employed in the development of bioactive compounds and materials science research, where its unique structure contributes to the design of novel polymers and advanced materials.

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