2-(tert-Butyl)thiophene-4-boronic acid pinacol ester

95%

Reagent Code: #89676
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CAS Number 2223054-49-5

science Other reagents with same CAS 2223054-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.2225 g/mol
Formula C₁₄H₂₅BO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it is employed in material science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronic devices such as organic light-emitting diodes (OLEDs) and solar cells.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿48,800.00
inventory 100mg
10-20 days ฿146,400.00

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2-(tert-Butyl)thiophene-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals.

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it is employed in material science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronic devices such as organic light-emitting diodes (OLEDs) and solar cells.

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