6-Morpholinopyridine-3-boronic acid

98%

Reagent Code: #90935
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CAS Number 904326-93-8

science Other reagents with same CAS 904326-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.03 g/mol
Formula C₉H₁₃BN₂O₃
badge Registry Numbers
MDL Number MFCD03086116
thermostat Physical Properties
Boiling Point 458.6°
inventory_2 Storage & Handling
Density 1.3g/mL
Storage  2-8°C

description Product Description

6-Morpholinopyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of bioactive compounds and drug candidates, where its morpholine and pyridine moieties contribute to enhanced solubility and binding affinity. Its versatility also extends to materials science, where it is used in the synthesis of organic electronic materials and polymers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿531.00
inventory 1g
10-20 days ฿1,449.00
inventory 5g
10-20 days ฿6,048.00

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6-Morpholinopyridine-3-boronic acid
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6-Morpholinopyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of bioac

6-Morpholinopyridine-3-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of bioactive compounds and drug candidates, where its morpholine and pyridine moieties contribute to enhanced solubility and binding affinity. Its versatility also extends to materials science, where it is used in the synthesis of organic electronic materials and polymers.

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