4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
96%
Reagent
Code: #242311
CAS Number
1195995-72-2
blur_circular Chemical Specifications
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Molecular Information
Weight
220.08 g/mol
Formula
C₁₁H₁₇BN₂O₂
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Registry Numbers
MDL Number
MFCD09607735
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Physical Properties
Boiling Point
364.8±27.0°C at 760 mmHg
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Storage & Handling
Storage
-20°C, sealed, dry
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 Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery for constructing complex nitrogen-containing heterocyclic systems. It is also employed in materials science for developing organic electronic materials, such as those used in OLEDs and semiconductors, due to its ability to introduce pyridine-based scaffolds with tailored electronic properties.
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
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 Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery for constructing complex nitrogen-containing heterocyclic systems. It is also employed in materials science for developing organic electronic materials, such as those used in OLEDs and semiconductors, due to its ability to introduce pyridine-based scaffolds with tailored electronic properties.
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