(3,5-Difluoro-2-nitrophenyl)boronic acid

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Reagent Code: #117253
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CAS Number 1150114-60-5

science Other reagents with same CAS 1150114-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.91 g/mol
Formula C₆H₄BF₂NO₄
badge Registry Numbers
MDL Number MFCD12025971
thermostat Physical Properties
Boiling Point 389.7±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.57±0.1 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

(3,5-Difluoro-2-nitrophenyl)boronic acid is primarily used in organic synthesis as a building block for creating more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds. This reaction is widely employed in the pharmaceutical industry to synthesize drug candidates and bioactive compounds. Additionally, its unique structure, featuring both nitro and fluoro substituents, makes it useful in the development of materials with specific electronic or optical properties. It also finds applications in the preparation of sensors and probes due to its ability to interact with various analytes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00

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(3,5-Difluoro-2-nitrophenyl)boronic acid
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(3,5-Difluoro-2-nitrophenyl)boronic acid is primarily used in organic synthesis as a building block for creating more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds. This reaction is widely employed in the pharmaceutical industry to synthesize drug candidates and bioactive compounds. Additionally, its unique structure, featuring both nitro and fluoro substituents, makes it useful in the development of materials with specific electronic or optical properties. It also finds applications in the preparation of sensors and probes due to its ability to interact with various analytes.
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