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

95%

Reagent Code: #90815
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CAS Number 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. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethylphenyl group enhances its reactivity and stability, making it suitable for creating compounds with specific electronic and steric properties. 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 Ft85,935.06
inventory 25mg
10-20 days Ft252,200.71
5-(4-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester
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. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethylphenyl group enhances its reactivity and stability, making it suitable for creating compounds with specific electronic and steric properties. Its application is also seen in the synthesis of bioactive molecules and functional materials, where precise molecular architecture is required.
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