5-N-Propylthiophene-2-Boronic Acid Pinacol Este

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Reagent Code: #90871
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CAS Number 1473358-18-7

science Other reagents with same CAS 1473358-18-7

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scatter_plot Molecular Information
Weight 252.19 g/mol
Formula C₁₃H₂₁BO₂S
badge Registry Numbers
MDL Number MFCD18436112
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for creating carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic ester group makes it a stable and effective reagent for introducing the thiophene moiety into complex molecules, enabling the development of compounds with specific electronic or structural properties. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its ability to facilitate the formation of thiophene-based architectures.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿28,080.00
inventory 100mg
10-20 days ฿87,120.00

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5-N-Propylthiophene-2-Boronic Acid Pinacol Este
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for creating carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic ester group makes it a stable and effective reagent for introducing the thiophene moiety into complex molecules, enabling the development of compounds with specific electronic or structural properties. Additionally, it finds application in the synthesis of con

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for creating carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic ester group makes it a stable and effective reagent for introducing the thiophene moiety into complex molecules, enabling the development of compounds with specific electronic or structural properties. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its ability to facilitate the formation of thiophene-based architectures.

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