1-Thianthrenylboronic acid
95%
- Product Code: 89496
Alias:
1-thianthraceneboronic acid
Thianthracene-1-boronic acid
CAS:
108847-76-3
| Molecular Weight: | 260.14 g./mol | Molecular Formula: | C₁₂H₉BO₂S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00093039 | |
| Melting Point: | 146-149 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
1-Thianthrenylboronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, incorporating a thianthrene moiety, can impart specific electronic properties to the resulting compounds, making it valuable in designing molecules with tailored functionalities. Additionally, it may serve as a building block in the development of organic semiconductors or ligands for catalysis, leveraging its boronic acid group for further functionalization or binding interactions.
Product Specification:
| Test | Specification |
|---|---|
| PURITYTITRATION WITH NAOH | 95 105% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿820.00 |
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| 5.000 | 10-20 days | ฿3,090.00 |
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| 25.000 | 10-20 days | ฿10,710.00 |
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1-Thianthrenylboronic acid
1-Thianthrenylboronic acid is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, incorporating a thianthrene moiety, can impart specific electronic properties to the resulting compounds, making it valuable in designing molecules with tailored functionalities. Additionally, it may serve as a building block in the development of organic semiconductors or ligands for catalysis, leveraging its boronic acid group for further functionalization or binding interactions.
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