6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one

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Reagent Code: #78592
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CAS Number 1207370-28-2

science Other reagents with same CAS 1207370-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.12 g/mol
Formula C₁₅H₁₈BNO₃
badge Registry Numbers
MDL Number MFCD18427677
thermostat Physical Properties
Boiling Point 454.2±45.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. It is also employed in material science for creating advanced polymers and organic electronic materials. Additionally, it serves as a key reagent in the synthesis of heterocyclic compounds, which are essential in agrochemical and medicinal chemistry research. Its stability and reactivity make it a preferred choice for functionalizing quinoline derivatives in various chemical processes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,329.00
inventory 250mg
10-20 days ฿13,041.00

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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one
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This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. It is also employed in material science for creating advanced polymers and organic electronic materials. Additionally, it serves as a key reagent in the synthesis of heterocyclic compounds, which are essenti

This compound is widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. It is also employed in material science for creating advanced polymers and organic electronic materials. Additionally, it serves as a key reagent in the synthesis of heterocyclic compounds, which are essential in agrochemical and medicinal chemistry research. Its stability and reactivity make it a preferred choice for functionalizing quinoline derivatives in various chemical processes.

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