(5-Chloro-2-fluoropyridin-3-yl)boronic acid

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Reagent Code: #90891
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CAS Number 937595-70-5

science Other reagents with same CAS 937595-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.35 g/mol
Formula C₅H₄BClFNO₂
badge Registry Numbers
MDL Number MFCD04972408
thermostat Physical Properties
Boiling Point 346.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with various aryl halides, facilitating the creation of complex organic molecules. It is also employed in the development of bioactive compounds, including potential drug candidates targeting specific biological pathways. Additionally, it finds use in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry and material science research.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,665.00
inventory 250mg
10-20 days ฿837.00
inventory 5g
10-20 days ฿6,021.00

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(5-Chloro-2-fluoropyridin-3-yl)boronic acid
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This chemical is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with various aryl halides, facilitating the creation of complex organic molecules. It is also employed in the development of bioactive compounds, including potential drug candidates targeting specific biological pathways. Additionally, it

This chemical is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with various aryl halides, facilitating the creation of complex organic molecules. It is also employed in the development of bioactive compounds, including potential drug candidates targeting specific biological pathways. Additionally, it finds use in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry and material science research.

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