2,3-Dichloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
Reagent
Code: #176200
CAS Number
741709-64-8
blur_circular Chemical Specifications
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Molecular Information
Weight
273.95 g/mol
Formula
C₁₁H₁₄BCl₂NO₂
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Registry Numbers
MDL Number
MFCD08063093
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Physical Properties
Boiling Point
354.9±42.0 °C
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Storage & Handling
Density
1.24±0.1 g/cm3
Storage
2-8°C, dry
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides under palladium catalysis. This makes it valuable in constructing complex pyridine-based structures commonly found in bioactive molecules. It is also employed in the development of organic electronic materials due to its ability to introduce chlorinated pyridine motifs into conjugated systems.
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