tert-Butyl methyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
96%
Reagent
Code: #52289
CAS Number
916587-44-5
blur_circular Chemical Specifications
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Molecular Information
Weight
333.2300 g/mol
Formula
C₁₈H₂₈BNO₄
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Registry Numbers
MDL Number
MFCD03490498
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Storage & Handling
Storage
room temperature
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a key intermediate. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its stability and reactivity under mild conditions. Additionally, it serves as a protecting group for amines in multi-step synthetic processes, ensuring selective transformations.
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