2-Methyl-5-(sec-butyl)thiophene-3-boronic acid pinacol ester

95%

Reagent Code: #89759
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CAS Number 2223006-79-7

science Other reagents with same CAS 2223006-79-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.24908 g/mol
Formula C₁₅H₂₇BO₃S
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 like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of heterocyclic compounds, which are often found in active pharmaceutical ingredients. Additionally, it is used in material science for the preparation of organic electronic materials, such as those used in OLEDs or organic semiconductors, due to its ability to introduce thiophene moieties into larger conjugated systems.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿96,000.00
inventory 100mg
10-20 days ฿285,000.00

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2-Methyl-5-(sec-butyl)thiophene-3-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of heterocyclic compounds, which are often found in active pharmaceutical ingredients. Additionally, it is used in material science for the preparation of organic electronic materials, such as those used in OLEDs or organic semiconductors, due to its ability to introduce thiophene moieties into larger conjugated systems.
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