(4-(Difluoromethyl)phenyl)boronic acid

97%

Reagent Code: #118854
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CAS Number 946525-43-5

science Other reagents with same CAS 946525-43-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.94 g/mol
Formula C₇H₇BF₂O₂
badge Registry Numbers
MDL Number MFCD09056705
thermostat Physical Properties
Boiling Point 287.0±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its difluoromethyl group enhances stability and reactivity, making it valuable for developing complex molecules. Also employed in material science for constructing advanced polymers and organic electronic materials. Its boronic acid moiety is crucial for binding to diols, enabling its use in sensors and diagnostic tools for detecting sugars and other biomolecules.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,630.00
inventory 1g
10-20 days ฿6,180.00
inventory 5g
10-20 days ฿20,290.00
inventory 250mg
10-20 days ฿1,960.00

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(4-(Difluoromethyl)phenyl)boronic acid
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Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its difluoromethyl group enhances stability and reactivity, making it valuable for developing complex molecules. Also employed in material science for constructing advanced polymers and organic electronic materials. Its boronic acid moiety is crucial for binding to diols, enabling its use in sensors and diagnostic tools for dete

Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its difluoromethyl group enhances stability and reactivity, making it valuable for developing complex molecules. Also employed in material science for constructing advanced polymers and organic electronic materials. Its boronic acid moiety is crucial for binding to diols, enabling its use in sensors and diagnostic tools for detecting sugars and other biomolecules.

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