4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
98%
- Product Code: 118575
CAS:
1010836-19-7
Molecular Weight: | 254.11 g./mol | Molecular Formula: | C₁₁H₁₅BO₄S |
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EC Number: | MDL Number: | MFCD08064045 | |
Melting Point: | Boiling Point: | 403.4±30.0 °C(Predicted) | |
Density: | 1.23±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating conjugated systems for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Additionally, it is employed in the synthesis of thiophene-based derivatives, which are widely used in materials science due to their optoelectronic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,971.00 |
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0.250 | 10-20 days | ฿3,339.00 |
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1.000 | 10-20 days | ฿9,000.00 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals, agrochemicals, and organic materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating conjugated systems for organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics. Additionally, it is employed in the synthesis of thiophene-based derivatives, which are widely used in materials science due to their optoelectronic properties.
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