(4-(3-(Dimethylamino)propoxy)-3-fluorophenyl)boronic acid hydrochloride
98%
- Product Code: 89242
CAS:
1704080-71-6
| Molecular Weight: | 277.53 g./mol | Molecular Formula: | C₁₁H₁₈BClFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400415 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. The dimethylamino and fluorine substituents enhance its reactivity and selectivity in these processes. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, serving as a key intermediate in the synthesis of complex molecules. Its water-soluble hydrochloride form ensures ease of handling and compatibility with various reaction conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | £931.37 |
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(4-(3-(Dimethylamino)propoxy)-3-fluorophenyl)boronic acid hydrochloride
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. Its structure, featuring a boronic acid group, enables it to form carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. The dimethylamino and fluorine substituents enhance its reactivity and selectivity in these processes. Additionally, it is employed in the development of pharmaceuticals and agrochemicals, serving as a key intermediate in the synthesis of complex molecules. Its water-soluble hydrochloride form ensures ease of handling and compatibility with various reaction conditions.
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