tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzylcarbamate
97%
Reagent
Code: #151664
CAS Number
832114-05-3
blur_circular Chemical Specifications
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Molecular Information
Weight
333.236 g/mol
Formula
C₁₈H₂₈BNO₄
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Registry Numbers
MDL Number
MFCD05863917
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Physical Properties
Melting Point
102-104 °C
Boiling Point
460.4±38.0 °C(Predicted)
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Storage & Handling
Density
1.06±0.1 g/cm3(Predicted)
Storage
2-8°C, sealed, dry
description Product Description
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its structure allows for the introduction of a protected benzylamine moiety into complex molecules, making it valuable in pharmaceutical and agrochemical synthesis. The Boc-protected amine group ensures compatibility with various reaction conditions and enables selective deprotection later in synthetic sequences. This compound is especially useful for constructing biaryl systems where amine functionality needs to be masked during transformation.
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