6-(Morpholinomethyl)pyridine-3-boronic Acid Pinacol Ester

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Reagent Code: #90941
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CAS Number 1160790-92-0

science Other reagents with same CAS 1160790-92-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.19 g/mol
Formula C₁₆H₂₅N₂O₃B
badge Registry Numbers
MDL Number MFCD16995640
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester moiety enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, it is employed in material science for creating organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in various chemical transformations.

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inventory 1g
10-20 days ฿27,590.00

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6-(Morpholinomethyl)pyridine-3-boronic Acid Pinacol Ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester moiety enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, it

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester moiety enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates. Additionally, it is employed in material science for creating organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in various chemical transformations.

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