5-(4-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90815
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CAS Number 2223029-20-5

science Other reagents with same CAS 2223029-20-5

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Weight 373.1981696 g/mol
Formula C₁₆H₁₉BF₃NO₃S
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. Its boronic ester group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential for constructing complex molecules. The thiazole ring and trifluoromethylphenyl group enhance its reactivity, stability, and biological activity, making it suitable for creating compounds with specific electronic, steric, and pharmacological properties. It is often employed in the development of pharmaceuticals targeting diseases such as cancer and infections, agrochemicals, and advanced materials. Its application is also seen in the synthesis of bioactive molecules and functional materials, where precise molecular architecture is required.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,280.00
inventory 25mg
10-20 days ฿24,300.00

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5-(4-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential for constructing complex molecules. The thiazole ring and trifluoromethylphenyl group enhance its reactivity, stability, and biological activity, making it suitable for creating compounds with specific electronic, steric, and pharmacological properties. It is often employed in the
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester group enables it to act as a key intermediate in forming carbon-carbon bonds, which is essential for constructing complex molecules. The thiazole ring and trifluoromethylphenyl group enhance its reactivity, stability, and biological activity, making it suitable for creating compounds with specific electronic, steric, and pharmacological properties. It is often employed in the development of pharmaceuticals targeting diseases such as cancer and infections, agrochemicals, and advanced materials. Its application is also seen in the synthesis of bioactive molecules and functional materials, where precise molecular architecture is required.
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