Thiophene-3-boronic acid, pinacol ester
96%
- Product Code: 91131
CAS:
214360-70-0
Molecular Weight: | 210.1 g./mol | Molecular Formula: | C₁₀H₁₅BO₂S |
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EC Number: | MDL Number: | MFCD05663893 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
Thiophene-3-boronic acid, pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing thiophene derivatives, which are essential in materials science for creating conductive polymers and organic semiconductors. Additionally, it is utilized in the production of agrochemicals and advanced materials due to its stability and reactivity in various chemical transformations.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white Solid |
PURITY | 95.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,410.00 |
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5.000 | 10-20 days | ฿5,540.00 |
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Thiophene-3-boronic acid, pinacol ester
Thiophene-3-boronic acid, pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing thiophene derivatives, which are essential in materials science for creating conductive polymers and organic semiconductors. Additionally, it is utilized in the production of agrochemicals and advanced materials due to its stability and reactivity in various chemical transformations.
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