N,N-Dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxamide

95%

Reagent Code: #91005
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CAS Number 1201644-42-9

science Other reagents with same CAS 1201644-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.14 g/mol
Formula C₁₄H₂₁BN₂O₃
badge Registry Numbers
MDL Number MFCD11878276
thermostat Physical Properties
Boiling Point 404.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage room temperature, inert gas

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 boronic ester derivative, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its pyridine moiety enhances stability and reactivity, making it suitable for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its application in medicinal chemistry is notable for creating bioactive compounds and drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,020.00
inventory 250mg
10-20 days ฿11,925.00
inventory 1g
10-20 days ฿32,175.00

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N,N-Dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxamide
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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 boronic ester derivative, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its pyridine moiety enhances stability and reactivity, making it suitable for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, such as pol

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester derivative, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its pyridine moiety enhances stability and reactivity, making it suitable for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its application in medicinal chemistry is notable for creating bioactive compounds and drug candidates.

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