3-Aminophenylboronic Acid Hemisulfate
98%(contains of Anhydride)
- Product Code: 90190
CAS:
66472-86-4
| Molecular Weight: | 185.98 g./mol | Molecular Formula: | C₆H₈BNO₂₁₂H₂SO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, inert gas storage |
Product Description:
Used as a key reagent in the synthesis of various organic compounds, particularly in cross-coupling reactions. It is widely employed in the preparation of pharmaceuticals, where it acts as a building block for drugs targeting diseases like cancer and diabetes. In biochemistry, it is utilized for the selective recognition and binding of carbohydrates, making it valuable in glucose sensing applications. Additionally, it plays a role in the development of advanced materials, such as polymers and sensors, due to its ability to form stable complexes with diols and other functional groups. Its versatility also extends to catalysis, where it aids in facilitating specific chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Amber to Dark green powder to crystal |
| Puritycontains of Anhydride | 97.5 100% |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿450.00 |
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| 5.000 | 10-20 days | ฿1,690.00 |
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| 25.000 | 10-20 days | ฿7,680.00 |
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3-Aminophenylboronic Acid Hemisulfate
Used as a key reagent in the synthesis of various organic compounds, particularly in cross-coupling reactions. It is widely employed in the preparation of pharmaceuticals, where it acts as a building block for drugs targeting diseases like cancer and diabetes. In biochemistry, it is utilized for the selective recognition and binding of carbohydrates, making it valuable in glucose sensing applications. Additionally, it plays a role in the development of advanced materials, such as polymers and sensors, due to its ability to form stable complexes with diols and other functional groups. Its versatility also extends to catalysis, where it aids in facilitating specific chemical transformations.
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