tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinoline-1(2H)-carboxylate
97%
Reagent
Code: #39699
CAS Number
1912446-60-6
blur_circular Chemical Specifications
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Molecular Information
Weight
359.27 g/mol
Formula
C₂₀H₃₀BNO₄
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Registry Numbers
MDL Number
MFCD11858571
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Storage & Handling
Storage
2-8°C, dry and sealed
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester functional group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the development of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it is used in materials science for the synthesis of advanced organic materials, where precise molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice in various synthetic pathways.
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