5-(2-Tolyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90770
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CAS Number 2223031-43-2

science Other reagents with same CAS 2223031-43-2

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

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, agrochemicals, and advanced materials. Additionally, it is utilized in the synthesis of thiazole-containing compounds, which are often explored for their biological activities, such as antimicrobial and anticancer properties. Its stability and reactivity make it a preferred choice in medicinal chemistry and material science research.

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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-(2-Tolyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, agrochemicals, and advanced materials. Additionally, it is utilized in the synthesis of thiazole-contain

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, agrochemicals, and advanced materials. Additionally, it is utilized in the synthesis of thiazole-containing compounds, which are often explored for their biological activities, such as antimicrobial and anticancer properties. Its stability and reactivity make it a preferred choice in medicinal chemistry and material science research.

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