3,5-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

97%

Reagent Code: #117257
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CAS Number 1029439-87-9

science Other reagents with same CAS 1029439-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.05 g/mol
Formula C₁₂H₁₅BF₂O₃
badge Registry Numbers
MDL Number MFCD22414561
thermostat Physical Properties
Boiling Point 338.3±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceuticals, agrochemicals, and material science. It serves as a key intermediate in the development of bioactive molecules and advanced materials. Its boronate ester group facilitates efficient and selective coupling with aryl halides, making it a versatile building block in medicinal chemistry and drug discovery. Additionally, it is employed in the synthesis of fluorescent dyes and sensors due to its unique electronic properties.

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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 250mg
10-20 days ฿2,601.00
inventory 1g
10-20 days ฿5,976.00
inventory 5g
10-20 days ฿23,238.00

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3,5-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceuticals, agrochemicals, and material science. It serves as a key intermediate in the development of bioactive molecules and advanced materials. Its boronate ester group facilitates efficient and selective coupling with aryl halides, making it a versatile building block in medicinal chemistry and drug discovery. Additionally, it is employed in the synthesis of fluorescent dyes and sensors due to its unique electronic properties.
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