(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methanol
98%
- Product Code: 37019
CAS:
1026796-39-3
| Molecular Weight: | 240.1300 g./mol | Molecular Formula: | C₁₁H₁₇BO₃S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The thiophene moiety enhances its utility in the synthesis of conjugated systems, which are essential in materials science for developing organic semiconductors, OLEDs, and other electronic materials. Additionally, the presence of the methanol group allows for further functionalization, expanding its applications in polymer chemistry and the creation of advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $96.80 |
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(5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methanol
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The thiophene moiety enhances its utility in the synthesis of conjugated systems, which are essential in materials science for developing organic semiconductors, OLEDs, and other electronic materials. Additionally, the presence of the methanol group allows for further functionalization, expanding its applications in polymer chemistry and the creation of advanced materials.
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