Potassium 2-Thienyltrifluoroborate
≥98%
- Product Code: 67356
CAS:
906674-55-3
| Molecular Weight: | 1903 g./mol | Molecular Formula: | C₄H₃BF₃KS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112719 | |
| Melting Point: | 253°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Potassium 2-Thienyltrifluoroborate is widely used in organic synthesis, particularly in cross-coupling reactions. It serves as a stable and efficient reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds between aryl or heteroaryl groups. This compound is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials science applications. Its stability and ease of handling make it a preferred choice in catalytic processes, contributing to the development of novel compounds with potential therapeutic or industrial uses. Additionally, it is employed in the preparation of thiophene derivatives, which are important in the production of organic semiconductors and conductive polymers.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | off white solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿570.00 |
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| 1.000 | 10-20 days | ฿1,380.00 |
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| 5.000 | 10-20 days | ฿5,990.00 |
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| 25.000 | 10-20 days | ฿21,360.00 |
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Potassium 2-Thienyltrifluoroborate
Potassium 2-Thienyltrifluoroborate is widely used in organic synthesis, particularly in cross-coupling reactions. It serves as a stable and efficient reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds between aryl or heteroaryl groups. This compound is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials science applications. Its stability and ease of handling make it a preferred choice in catalytic processes, contributing to the development of novel compounds with potential therapeutic or industrial uses. Additionally, it is employed in the preparation of thiophene derivatives, which are important in the production of organic semiconductors and conductive polymers.
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