4-(3-Furyl)thiazole-5-boronic acid pinacol ester

95%

Reagent Code: #90384
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CAS Number 2223030-77-9

science Other reagents with same CAS 2223030-77-9

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Weight 295.16232 g/mol
Formula C₁₃H₁₈BNO₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds like heterocycles and biologically active molecules. Additionally, it is employed in material science for developing organic electronic materials and polymers. Its furyl and thiazole moieties contribute to its utility in creating compounds with potential applications in drug discovery and functional materials.

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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-(3-Furyl)thiazole-5-boronic acid pinacol ester
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds like heterocycles and biologically active molecules. Additionally, it is employed in material science for developing organic

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse compounds like heterocycles and biologically active molecules. Additionally, it is employed in material science for developing organic electronic materials and polymers. Its furyl and thiazole moieties contribute to its utility in creating compounds with potential applications in drug discovery and functional materials.

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