1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone

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Reagent Code: #114601
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CAS Number 1227068-67-8

science Other reagents with same CAS 1227068-67-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.13 g/mol
Formula C₁₃H₂₂BNO₃
badge Registry Numbers
MDL Number MFCD18427628
inventory_2 Storage & Handling
Density 1.1±0.1 g/cm3
Storage -20°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed to introduce specific functional groups into target molecules, aiding in the creation of bioactive compounds or advanced materials. Additionally, it serves as a key building block in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for drug discovery and development. Its stability and reactivity make it a preferred choice for researchers working on precision chemical transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,188.00
inventory 100mg
10-20 days ฿774.00
inventory 5g
10-20 days ฿12,546.00
inventory 1g
10-20 days ฿2,556.00

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1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridin-1(2H)-yl)ethanone
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed to introduce specific functional groups into target molecules, aiding in the creation of bioactive compounds or advanced materials. Additionally, it serves as a key building block in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry for drug discovery and development. Its stability and reactivity make it a preferred choice for researchers working on precision chemical transformations.
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