2-Bromo-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
95%
Reagent
Code: #46557
CAS Number
863118-14-3
blur_circular Chemical Specifications
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Molecular Information
Weight
340.02 g/mol
Formula
C₁₄H₁₉BBrNO₃
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Registry Numbers
MDL Number
MFCD18783181
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Physical Properties
Boiling Point
461.4±30.0 °C
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Storage & Handling
Density
1.33±0.1 g/cm3
Storage
2-8°C, dry
description Product Description
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in the field of medicinal chemistry. Its boronate ester functional group makes it valuable for Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Additionally, the bromoacetamide moiety allows for further functionalization, enabling the introduction of various substituents to tailor the properties of the final product. Its application extends to the development of bioactive compounds, including potential drug candidates targeting specific biological pathways.
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