3-Cyano-4-fluorophenylboronic acid, pinacol ester

≥98%

Reagent Code: #90220
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CAS Number 775351-57-0

science Other reagents with same CAS 775351-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.08 g/mol
Formula C₁₃H₁₅BFNO₂
badge Registry Numbers
MDL Number MFCD06795681
thermostat Physical Properties
Boiling Point 334.5ºC
inventory_2 Storage & Handling
Density 1.12g/cm3
Storage room temperature, dry

description Product Description

This chemical is commonly used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is utilized in materials science for creating advanced polymers and electronic materials. The presence of both cyano and fluoro groups enhances its reactivity and selectivity in various chemical transformations.

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Test Parameter Specification
Appearance White to Almost white powder to crystal
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿330.00
inventory 1g
10-20 days ฿1,330.00
inventory 5g
10-20 days ฿4,240.00

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3-Cyano-4-fluorophenylboronic acid, pinacol ester
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This chemical is commonly used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is utilized in materials science for creating advanced polymers and electronic materials. The presence of both cyano and fluoro groups enhances its reactivity and selectivity in various chemical transformations.
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