5-(3,5-Difluorophenyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90775
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CAS Number 1402227-88-6

science Other reagents with same CAS 1402227-88-6

blur_circular Chemical Specifications

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Weight 340.1930664 g/mol
Formula C₁₆H₁₉BF₂O₃S
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 organic molecules, especially those containing thiophene and difluorophenyl moieties. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials. The boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to the unique electronic properties of thiophene derivatives.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(3,5-Difluorophenyl)thiophene-2-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 organic molecules, especially those containing thiophene and difluorophenyl moieties. Its application is significant in the development of pharmaceuticals, agrochemicals, and advanced materials. The boronic ester group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to the unique electronic properties of thiophene derivatives.
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