4-(3,5-Difluorophenyl)thiazole-5-boronic acid pinacol ester

95%

Reagent Code: #90373
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CAS Number 2223050-83-5

science Other reagents with same CAS 2223050-83-5

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Weight 341.1811264 g/mol
Formula C₁₅H₁₈BF₂NO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Its boronic ester group enables efficient coupling with aryl or vinyl halides, making it valuable in constructing biaryl or related compounds. The 3,5-difluorophenyl and thiazole moieties enhance its utility in medicinal chemistry by influencing the biological activity of resulting molecules, targeting specific biological pathways in drug candidate development. Also utilized in the synthesis of advanced materials, such as organic semiconductors, due to its ability to form stable carbon-carbon bonds.

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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-(3,5-Difluorophenyl)thiazole-5-boronic acid pinacol ester
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Its boronic ester group enables efficient coupling with aryl or vinyl halides, making it valuable in constructing biaryl or related compounds. The 3,5-difluorophenyl and thiazole moieties enhance its utility in medicinal chemistry by influencing the biological activity of resulting molecules, targeting specific biological pathways in drug candidate dev

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex molecules for pharmaceuticals and materials science. Its boronic ester group enables efficient coupling with aryl or vinyl halides, making it valuable in constructing biaryl or related compounds. The 3,5-difluorophenyl and thiazole moieties enhance its utility in medicinal chemistry by influencing the biological activity of resulting molecules, targeting specific biological pathways in drug candidate development. Also utilized in the synthesis of advanced materials, such as organic semiconductors, due to its ability to form stable carbon-carbon bonds.

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