Thiophene-2-boronic acid pinacol ester
97%
- Product Code: 91130
Alias:
Thiophene-2-boronic acid pinacol ester 2-thiophene boric acid pinacol ester
CAS:
193978-23-3
Molecular Weight: | 210.1 g./mol | Molecular Formula: | C₁₀H₁₅BO₂S |
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EC Number: | MDL Number: | MFCD05663878 | |
Melting Point: | 68-70°C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
Thiophene-2-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Its stability and reactivity make it a preferred choice in the development of electronic materials, such as organic semiconductors and conductive polymers. Additionally, it is employed in the creation of ligands for catalysis and in the modification of polymers to enhance their properties. Its applications extend to research and development in medicinal chemistry, where it aids in the design of novel drug candidates.
Product Specification:
Test | Specification |
---|---|
PURITY GC | 96.5 100% |
SULFUR | 14.5-16 |
APPEARANCE | White to beige powder or crystals |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿270.00 |
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5.000 | 10-20 days | ฿610.00 |
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25.000 | 10-20 days | ฿2,880.00 |
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Thiophene-2-boronic acid pinacol ester
Thiophene-2-boronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including heterocyclic compounds. Its stability and reactivity make it a preferred choice in the development of electronic materials, such as organic semiconductors and conductive polymers. Additionally, it is employed in the creation of ligands for catalysis and in the modification of polymers to enhance their properties. Its applications extend to research and development in medicinal chemistry, where it aids in the design of novel drug candidates.
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