5-(4-Tolyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90813
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CAS Number 2223044-52-6

science Other reagents with same CAS 2223044-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.22678 g/mol
Formula C₁₆H₂₂BNO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,280.00
inventory 25mg
10-20 days ฿24,300.00

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5-(4-Tolyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additi

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.

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