2-Aminophenylboronic acid hydrochloride
97%
- Product Code: 91222
Alias:
Anthranilic borate hydrochloride
CAS:
863753-30-4
| Molecular Weight: | 173.41 g./mol | Molecular Formula: | NH₂C₆H₄BOH₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02258096 | |
| Melting Point: | 115-118°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and functional materials. Its boronic acid group enables efficient conjugation with diols, making it valuable in carbohydrate chemistry and sensor development. Additionally, it is employed in the preparation of boron-containing polymers and as a ligand in catalysis. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction environments.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97-100 |
| PURITYTITRATION WITH AGNO3 | 97-100 |
| APPEARANCE | White to tan powder or crystals |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿380.00 |
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| 1.000 | 10-20 days | ฿1,300.00 |
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| 5.000 | 10-20 days | ฿4,500.00 |
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| 25.000 | 10-20 days | ฿16,680.00 |
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2-Aminophenylboronic acid hydrochloride
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and functional materials. Its boronic acid group enables efficient conjugation with diols, making it valuable in carbohydrate chemistry and sensor development. Additionally, it is employed in the preparation of boron-containing polymers and as a ligand in catalysis. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction environments.
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