5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
98%
- Product Code: 61035
Alias:
5-Formylthiophene-2-boronic acid pinacol ester; 5-Formyl-2-thiopheneboronic acid pinacol ester
CAS:
1040281-83-1
| Molecular Weight: | 238.11 g./mol | Molecular Formula: | C₁₁H₁₅BO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09266186 | |
| Melting Point: | Boiling Point: | 359.1±27.0°C | |
| Density: | Storage Condition: | 2-8°C, inert gas atmosphere |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is used in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its thiophene moiety, which contributes to electronic properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿270.00 |
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| 1.000 | 10-20 days | ฿340.00 |
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| 5.000 | 10-20 days | ฿1,500.00 |
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| 25.000 | 10-20 days | ฿7,340.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is used in the synthesis of conjugated polymers and small molecules for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its thiophene moiety, which contributes to electronic properties.
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