5-(4-Bromopyridin-2-yl)furan-2-boronic acid

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Reagent Code: #92242
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CAS Number 2225176-10-1

science Other reagents with same CAS 2225176-10-1

blur_circular Chemical Specifications

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Weight 267.87178 g/mol
Formula C₉H₇BBrNO₃
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 the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl or heteroaryl structures, while the 4-bromopyridin-2-yl substituent allows for additional orthogonal functionalization or sequential coupling reactions. This makes it valuable in the synthesis of active pharmaceutical ingredients (APIs) and intermediates for drug discovery. Additionally, it is used in material science for the development of organic electronic materials, where its pyridine and furan moieties contribute to the desired electronic properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿13,400.00
inventory 25mg
10-20 days ฿40,200.00
inventory 100mg
10-20 days ฿120,600.00

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5-(4-Bromopyridin-2-yl)furan-2-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl or heteroaryl structures, while the 4-bromopyridin-2-yl substituent allows for additional orthogonal functionalization or se
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl or heteroaryl structures, while the 4-bromopyridin-2-yl substituent allows for additional orthogonal functionalization or sequential coupling reactions. This makes it valuable in the synthesis of active pharmaceutical ingredients (APIs) and intermediates for drug discovery. Additionally, it is used in material science for the development of organic electronic materials, where its pyridine and furan moieties contribute to the desired electronic properties.
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