2-(2,5-Dibromothiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 61564
CAS:
942070-22-6
| Molecular Weight: | 367.89 g./mol | Molecular Formula: | C₁₀H₁₃BBr₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12405469 | |
| Melting Point: | Boiling Point: | 371°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the development of drugs, agrochemicals, and advanced materials like organic semiconductors. Additionally, it is utilized in the synthesis of thiophene-based compounds, which are important in electronic and optoelectronic applications due to their conductive and luminescent properties.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97-100 |
| APPEARANCE | SOLID |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿780.00 |
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| 1.000 | 10-20 days | ฿2,680.00 |
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| 5.000 | 10-20 days | ฿9,400.00 |
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2-(2,5-Dibromothiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the development of drugs, agrochemicals, and advanced materials like organic semiconductors. Additionally, it is utilized in the synthesis of thiophene-based compounds, which are important in electronic and optoelectronic applications due to their conductive and luminescent properties.
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