4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrazole

95%

Reagent Code: #90417
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CAS Number 1391835-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.23 g/mol
Formula C₁₆H₂₁BN₂O₄S
badge Registry Numbers
MDL Number MFCD22571831
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tosyl-protected pyrazole and a dioxaborolane group, makes it valuable for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are essential in materials science and agrochemical applications. Its versatility and efficiency in coupling reactions make it a useful tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days £76.75
inventory 250mg
10-20 days £139.48
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrazole
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a tosyl-protected pyrazole and a dioxaborolane group, makes it valuable for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its stability and reactivity. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are essential in materials science and agrochemical applications. Its versatility and efficiency in coupling reactions make it a useful tool in modern synthetic chemistry.
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