2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)aniline
95%
Reagent
Code: #62323
CAS Number
1058062-64-8
blur_circular Chemical Specifications
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Molecular Information
Weight
287.09 g/mol
Formula
C₁₃H₁₇BF₃NO₂
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Registry Numbers
MDL Number
MFCD16996235
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Storage & Handling
Storage
2-8°C, away from light, dry, sealed
description Product Description
This compound is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals due to its boronic ester functional group, which facilitates Suzuki-Miyaura coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, its trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it valuable in drug discovery and development. It is also employed in material science for the synthesis of advanced organic materials with specific electronic or optical properties.
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