1-Phenyl-5-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-yl)-1H-Pyrazole

≥97%

Reagent Code: #89515
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CAS Number 1238702-58-3

science Other reagents with same CAS 1238702-58-3

blur_circular Chemical Specifications

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Weight 270.14 g/mol
Formula C₁₅H₁₉BN₂O₂
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. Its boronate ester group makes it a valuable building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it is used in materials science for the development of advanced polymers and organic electronic materials, where precise molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice for researchers in these fields.

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inventory 250mg
10-20 days ฿1,197.00

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1-Phenyl-5-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-yl)-1H-Pyrazole
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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 building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it is used in

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 building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds. Additionally, it is used in materials science for the development of advanced polymers and organic electronic materials, where precise molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice for researchers in these fields.

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