(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanamine
95%
Reagent
Code: #242873
CAS Number
248274-04-6
blur_circular Chemical Specifications
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Molecular Information
Weight
233.12 g/mol
Formula
C₁₃H₂₀BNO₂
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Registry Numbers
MDL Number
MFCD16295106
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Physical Properties
Boiling Point
352.1±25.0 °C(Predicted)
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Storage & Handling
Density
1.03±0.1 g/cm3(Predicted)
Storage
2-8°C, light-proof storage, inert atmosphere
description Product Description
Widely used in organic synthesis, particularly as a building block in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables efficient carbon-carbon bond formation with aryl or vinyl halides, making it valuable in the preparation of complex aromatic compounds. The presence of a primary amine group allows for further functionalization, such as amide bond formation or reductive amination, enabling its use in medicinal chemistry for drug discovery and development. It is also employed in the synthesis of functional materials, including conjugated polymers and ligands for catalysts. Its dual functionality makes it a versatile intermediate in multi-step syntheses.
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