1-Benzothiophen-2-ylboronic acid
98%
- Product Code: 91211
Alias:
Benzothiophene-2-boronic acid
CAS:
98437-23-1
| Molecular Weight: | 178.02 g./mol | Molecular Formula: | C₈H₇BO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01075674 | |
| Melting Point: | 254-256 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is widely 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. The boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing various heterocyclic compounds. It is also employed in the development of materials for organic electronics, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its ability to modify electronic properties. Additionally, it finds applications in the preparation of bioactive molecules and agrochemicals, contributing to the discovery of new drugs and crop protection agents.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 250-260 |
| Purity | 98-100 |
| APPEARANCE | WHITE TO OFF-WHITE TO LIGHT BROWN POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿520.00 |
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| 5.000 | 10-20 days | ฿1,590.00 |
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| 25.000 | 10-20 days | ฿7,350.00 |
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1-Benzothiophen-2-ylboronic acid
This compound is widely 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. The boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable for synthesizing various heterocyclic compounds. It is also employed in the development of materials for organic electronics, such as organic light-emitting diodes (OLEDs) and semiconductors, due to its ability to modify electronic properties. Additionally, it finds applications in the preparation of bioactive molecules and agrochemicals, contributing to the discovery of new drugs and crop protection agents.
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