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

95%

Reagent Code: #90774
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CAS Number 2223039-36-7

science Other reagents with same CAS 2223039-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.1811264 g/mol
Formula C₁₅H₁₈BF₂NO₃S
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 pharmaceutical and materials science fields. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Researchers often employ it in the development of drug candidates, where its difluorophenyl and thiazole moieties contribute to specific pharmacological properties. Additionally, it can be used in the synthesis of organic electronic materials, where its structural features enhance performance characteristics.

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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-(3,5-Difluorophenyl)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 pharmaceutical and materials science fields. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Researchers often employ it in the development of drug candidates, where its difluoroph

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 pharmaceutical and materials science fields. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds or advanced materials. Researchers often employ it in the development of drug candidates, where its difluorophenyl and thiazole moieties contribute to specific pharmacological properties. Additionally, it can be used in the synthesis of organic electronic materials, where its structural features enhance performance characteristics.

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