5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole
97%
- Product Code: 241639
CAS:
1073354-91-2
| Molecular Weight: | 261.15 g./mol | Molecular Formula: | C₁₃H₁₆BNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09260439 | |
| Melting Point: | Boiling Point: | 380.6±15.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and organic electronic materials. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl and heteroaryl structures found in bioactive molecules. It is particularly valuable in drug discovery for constructing complex thiazole-containing scaffolds. Additionally, it finds use in materials science for developing fluorescent dyes and organic semiconductors due to the electron-accepting nature of the benzo[d]thiazole core.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft2,015.82 |
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| 0.250 | 10-20 days | Ft3,527.69 |
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| 1.000 | 10-20 days | Ft21,628.11 |
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| 5.000 | 10-20 days | Ft87,982.30 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and organic electronic materials. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl and heteroaryl structures found in bioactive molecules. It is particularly valuable in drug discovery for constructing complex thiazole-containing scaffolds. Additionally, it finds use in materials science for developing fluorescent dyes and organic semiconductors due to the electron-accepting nature of the benzo[d]thiazole core.
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