3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
95%
Reagent
Code: #242533
CAS Number
1073354-97-8
blur_circular Chemical Specifications
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Molecular Information
Weight
220.07 g/mol
Formula
C₁₁H₁₇BN₂O₂
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Registry Numbers
MDL Number
MFCD09260488
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Storage & Handling
Storage
-20°C, inflatable, avoiding light
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery and development, especially for constructing complex nitrogen-containing heterocyclic systems. It is also employed in materials science for designing organic electronic materials due to its stable and reactive boronate ester functionality.
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