4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
95%
- Product Code: 87437
CAS:
1088118-97-1
| Molecular Weight: | 262.14 g./mol | Molecular Formula: | C₁₂H₁₅BN₂O₂S |
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| EC Number: | MDL Number: | MFCD21604133 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed 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 ability to enhance charge transport properties. Its benzo[c][1,2,5]thiadiazole moiety also contributes to its use in designing fluorescent probes and sensors for detecting specific analytes in biological and environmental systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £167.93 |
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| 0.250 | 10-20 days | £324.67 |
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| 1.000 | 10-20 days | £809.94 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed 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 ability to enhance charge transport properties. Its benzo[c][1,2,5]thiadiazole moiety also contributes to its use in designing fluorescent probes and sensors for detecting specific analytes in biological and environmental systems.
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