(7-Chloro-2-(2-Methyl-3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Benzo[D]Oxazol-5-Yl)Methanol
97%
Reagent
Code: #165689
CAS Number
2230904-26-2
blur_circular Chemical Specifications
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Molecular Information
Weight
399.68 g/mol
Formula
C₂₁H₂₃BClNO₄
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Storage & Handling
Storage
Room temperature
description Product Description
Used primarily as an intermediate in pharmaceutical synthesis, this compound plays a key role in Suzuki-Miyaura cross-coupling reactions due to the presence of the boronate ester group. It enables the formation of biaryl structures, which are common motifs in drug development. Its hydroxyl functionality allows for further derivatization, making it valuable in constructing complex organic molecules, particularly in the discovery of new therapeutic agents. It is often employed in research settings for the development of novel compounds with potential biological activity.
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