5-Bromo-2-(1H-imidazol-1-yl)phenylboronic acid

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Reagent Code: #90860
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CAS Number 2225173-63-5

science Other reagents with same CAS 2225173-63-5

blur_circular Chemical Specifications

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Weight 266.88702 g/mol
Formula C₉H₈BBrN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients (APIs). Additionally, it is employed in the development of advanced materials, such as organic electronic compounds, due to its ability to form stable and functionalized aromatic systems. Its imidazole moiety also contributes to its use in designing molecules with potential biological activity, particularly in drug discovery for targeting enzymes or receptors.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿16,182.00
inventory 25mg
10-20 days ฿46,782.00

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5-Bromo-2-(1H-imidazol-1-yl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients (APIs). Additionally, it is employed in the development of advanced materials, su

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients (APIs). Additionally, it is employed in the development of advanced materials, such as organic electronic compounds, due to its ability to form stable and functionalized aromatic systems. Its imidazole moiety also contributes to its use in designing molecules with potential biological activity, particularly in drug discovery for targeting enzymes or receptors.

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