N-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
98%
Reagent
Code: #116954
CAS Number
1005009-98-2
science Other reagents with same CAS 1005009-98-2
blur_circular Chemical Specifications
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Molecular Information
Weight
234.1 g/mol
Formula
C₁₂H₁₉BN₂O₂
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Registry Numbers
MDL Number
MFCD11878220
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Physical Properties
Boiling Point
352.7±27.0 °C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, inert gas
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and materials for electronic applications due to its stability and reactivity.
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