5-(Diethylamino)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90827
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CAS Number 2223046-09-9

science Other reagents with same CAS 2223046-09-9

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Weight 299.23714 g/mol
Formula C₁₄H₂₆BNO₃S
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 building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it is used in materials science for the development of organic electronic materials, such as conductive polymers and organic light-emitting diodes (OLEDs), due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,602.00

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5-(Diethylamino)thiophene-2-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 building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their potential biological activities, including antimicrobial,

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it is used in materials science for the development of organic electronic materials, such as conductive polymers and organic light-emitting diodes (OLEDs), due to the electron-rich nature of the thiophene ring.

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