N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)butan-1-amine
96%
Reagent
Code: #219617
CAS Number
1256359-08-6
blur_circular Chemical Specifications
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Molecular Information
Weight
289.22 g/mol
Formula
C₁₇H₂₈BNO₂
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Registry Numbers
MDL Number
MFCD14280318
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Physical Properties
Boiling Point
390.6±25.0 °C(Predicted)
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Storage & Handling
Density
0.98±0.1 g/cm3(Predicted)
Storage
Room temperature, inert gas
description Product Description
Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The presence of a benzylamine moiety allows for further functionalization, supporting its use in the development of bioactive compounds and functional materials. Its structure is particularly useful in medicinal chemistry for constructing nitrogen-containing scaffolds.
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