4-Fluoro-2-(cyclopropyl)pyridine-5-boronic acid

95%

Reagent Code: #92153
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CAS Number 2225179-54-2

science Other reagents with same CAS 2225179-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.9719632 g/mol
Formula C₈H₉BFNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key building block for introducing the cyclopropylpyridine moiety into more complex molecules, which are often explored in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds with potential biological activity. Its applications are mainly focused on drug discovery and development, where it aids in creating novel therapeutic agents. Additionally, it may be used in material science for designing advanced organic materials with specific properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,520.00
inventory 100mg
10-20 days ฿135,200.00
inventory 25mg
10-20 days ฿45,060.00

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4-Fluoro-2-(cyclopropyl)pyridine-5-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key building block for introducing the cyclopropylpyridine moiety into more complex molecules, which are often explored in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds with potential biological activity. Its applications are mainly focused on drug discovery and de

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key building block for introducing the cyclopropylpyridine moiety into more complex molecules, which are often explored in pharmaceutical research. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds with potential biological activity. Its applications are mainly focused on drug discovery and development, where it aids in creating novel therapeutic agents. Additionally, it may be used in material science for designing advanced organic materials with specific properties.

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