5-Formyl-2-thiopheneboronic acid
97%
- Product Code: 90929
Alias:
5-formyl-2-thiophene boronic acid ;5-formylthiophene-2-boronic acid, 5-formylthiophene-2-boronic acid
CAS:
4347-33-5
| Molecular Weight: | 155.97 g./mol | Molecular Formula: | C₅H₅BO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093666 | |
| Melting Point: | 132-135 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The formyl group on the thiophene ring allows for further functionalization, making it versatile in designing molecules with specific properties. Additionally, it finds application in material science for synthesizing conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and other advanced materials. Its boronic acid moiety enables efficient cross-coupling with aryl halides, facilitating the construction of carbon-carbon bonds in a controlled manner.
Product Specification:
| Test | Specification |
|---|---|
| PURITYNEUTRALIZATION TITRATION | 96.5 103.5% |
| APPEARANCE | YELLOW TO ORANGE TO BROWN POWDER OR CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿550.00 |
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| 5.000 | 10-20 days | ฿1,550.00 |
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| 25.000 | 10-20 days | ฿5,860.00 |
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| 100.000 | 10-20 days | ฿22,700.00 |
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5-Formyl-2-thiopheneboronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The formyl group on the thiophene ring allows for further functionalization, making it versatile in designing molecules with specific properties. Additionally, it finds application in material science for synthesizing conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and other advanced materials. Its boronic acid moiety enables efficient cross-coupling with aryl halides, facilitating the construction of carbon-carbon bonds in a controlled manner.
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