3-Bromo-5-(thiazol-4-yl)phenylboronic acid

95%

Reagent Code: #91897
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CAS Number 2225172-78-9

science Other reagents with same CAS 2225172-78-9

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Weight 283.93738 g/mol
Formula C₉H₇BBrNO₂S
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional moiety, enabling the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, the thiazole moiety in its structure can contribute to the biological activity of the resulting compounds, making it useful in drug discovery and development. Its applications also extend to the creation of complex organic molecules for research and industrial purposes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿48,600.00

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3-Bromo-5-(thiazol-4-yl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional moiety, enabling the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, the thiazole moiety in its structure can contribute to the biological activity of the resulting compounds, making it useful in drug discovery and development. Its applications also extend to the creation of complex organic molecules for research and industrial purposes.
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