4-(Dimethylamino)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90488
CAS:
2223029-68-1
Molecular Weight: | 271.18398 g./mol | Molecular Formula: | C₁₂H₂₂BNO₃S |
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Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of thiophene derivatives into more complex molecules, which are often used in the development of pharmaceuticals, agrochemicals, and organic electronic materials. Its boronic ester functionality allows for efficient and selective coupling with aryl or vinyl halides, enabling the creation of diverse organic structures. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for use in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), where thiophene-based compounds are valued for their electronic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | ฿15,552.00 |
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0.100 | 10-20 days | ฿46,602.00 |
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4-(Dimethylamino)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of thiophene derivatives into more complex molecules, which are often used in the development of pharmaceuticals, agrochemicals, and organic electronic materials. Its boronic ester functionality allows for efficient and selective coupling with aryl or vinyl halides, enabling the creation of diverse organic structures. Additionally, it finds application in the synthesis of conjugated polymers and small molecules for use in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), where thiophene-based compounds are valued for their electronic properties.
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