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

95%

Reagent Code: #90768
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CAS Number 2223041-57-2

science Other reagents with same CAS 2223041-57-2

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

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates efficient coupling with aryl or vinyl halides, making it valuable for constructing complex organic molecules. Additionally, it finds application in the development of conjugated polymers and organic electronic materials due to its ability to introduce thiophene units, which are essential for enhancing electronic properties. Its stability and reactivity make it a preferred choice in research and industrial processes requiring precise molecular assembly.

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

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5-(2-Methylpropyl)thiophene-2-boronic acid pinacol ester
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates efficient coupling with aryl or vinyl halides, making it valuable for constructing complex organic molecules. Additionally, it finds application in the development of conjugated polymers and organic electronic materials due to its abili

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates efficient coupling with aryl or vinyl halides, making it valuable for constructing complex organic molecules. Additionally, it finds application in the development of conjugated polymers and organic electronic materials due to its ability to introduce thiophene units, which are essential for enhancing electronic properties. Its stability and reactivity make it a preferred choice in research and industrial processes requiring precise molecular assembly.

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