N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)cyclopropanecarboxamide
98%
Reagent
Code: #50152
CAS Number
1286230-87-2
blur_circular Chemical Specifications
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Molecular Information
Weight
288.14984 g/mol
Formula
C₁₅H₂₁BN₂O₃
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Registry Numbers
MDL Number
MFCD16995630
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it finds application in materials science for the preparation of advanced organic materials, such as polymers and ligands for catalysis. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.
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