4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-pyrazole
95%
Reagent
Code: #90417
CAS Number
1391835-53-2
blur_circular Chemical Specifications
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Molecular Information
Weight
348.23 g/mol
Formula
C₁₆H₂₁BN₂O₄S
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Registry Numbers
MDL Number
MFCD22571831
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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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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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