2-(iso-Propyl)thiophene-4-boronic acid pinacol ester

95%

Reagent Code: #89649
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CAS Number 2223050-93-7

science Other reagents with same CAS 2223050-93-7

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scatter_plot Molecular Information
Weight 270.19592 g/mol
Formula C₁₃H₂₃BO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

2-(iso-Propyl)thiophene-4-boronic acid pinacol ester is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a crucial intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It enables the formation of carbon-carbon bonds, facilitating the synthesis of various thiophene derivatives, which are valuable in drug development and material science. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and conductive polymers, due to its ability to introduce thiophene moieties into molecular structures. Its stability and reactivity make it a versatile tool in advanced chemical research and industrial applications.

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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-(iso-Propyl)thiophene-4-boronic acid pinacol ester
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2-(iso-Propyl)thiophene-4-boronic acid pinacol ester is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a crucial intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It enables the formation of carbon-carbon bonds, facilitating the synthesis of various thiophene derivatives, which are valuable in drug development and material science. Additionally, it is employed in the

2-(iso-Propyl)thiophene-4-boronic acid pinacol ester is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a crucial intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. It enables the formation of carbon-carbon bonds, facilitating the synthesis of various thiophene derivatives, which are valuable in drug development and material science. Additionally, it is employed in the production of organic electronic materials, such as semiconductors and conductive polymers, due to its ability to introduce thiophene moieties into molecular structures. Its stability and reactivity make it a versatile tool in advanced chemical research and industrial applications.

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