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

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Reagent Code: #90425
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CAS Number 2223053-49-2

science Other reagents with same CAS 2223053-49-2

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Weight 339.64526 g/mol
Formula C₁₅H₁₉BClNO₃S
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 like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. This is essential in synthesizing bioactive compounds, agrochemicals, and advanced materials. Additionally, it finds use in the preparation of thiazole derivatives, which are important in designing drugs with antimicrobial, anti-inflammatory, or anticancer properties. Its stability and reactivity make it a preferred choice for chemists working on targeted molecular frameworks.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00

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4-(4-Chlorophenyl)thiazole-5-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. This is essential in synthesizing bioactive compounds, agrochemicals, and advanced materials. Additionally, it finds use in the preparation of thiazole derivatives, which are important in designing drugs with antimicrobial, anti-inflammatory, or anticancer properties. Its stability and reactivity make it a preferred choice for chemists working on targeted molecular frameworks.
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