4-(N,N-DiMethylaMino)Phenylboronic Acid Hydrochloride
98%
- Product Code: 60918
Alias:
4-Dimethylaminophenylboronic acid 4-Dimethylaminophenylboronic acid 4-(N,N-dimethylamino)phenylboronic acid 4-(N,N-dimethylamino)phenylboronic acid
CAS:
1150114-73-0
| Molecular Weight: | 201.45832 g./mol | Molecular Formula: | C₈H₁₃BClNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds efficiently. It is also employed in the preparation of pharmaceutical intermediates and bioactive molecules due to its stability and reactivity. Additionally, it serves as a building block in the development of sensors and probes for detecting sugars and other analytes in biochemical research. Its boronic acid group enables it to interact with diols, making it useful in carbohydrate chemistry and glycobiology studies.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| MELTING POINT | 123-130 |
| APPEARANCE | White to off white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $29.63 |
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| 1.000 | 10-20 days | $131.09 |
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| 5.000 | 10-20 days | $361.63 |
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4-(N,N-DiMethylaMino)Phenylboronic Acid Hydrochloride
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds efficiently. It is also employed in the preparation of pharmaceutical intermediates and bioactive molecules due to its stability and reactivity. Additionally, it serves as a building block in the development of sensors and probes for detecting sugars and other analytes in biochemical research. Its boronic acid group enables it to interact with diols, making it useful in carbohydrate chemistry and glycobiology studies.
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