N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-phenylacetamide
95%
Reagent
Code: #83678
CAS Number
2045409-68-3
blur_circular Chemical Specifications
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Molecular Information
Weight
367.2464 g/mol
Formula
C₂₁H₂₆BNO₄
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Registry Numbers
MDL Number
MFCD32206525
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it serves as a key building block in the preparation of advanced materials, such as organic semiconductors or polymers, where precise molecular architecture is required. Its application extends to medicinal chemistry, where it aids in the creation of targeted therapies and drug discovery efforts.
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