(4-(1-(Cyclopropylamino)ethyl)phenyl)boronic acid hydrochloride
98%
- Product Code: 89221
CAS:
1704073-39-1
| Molecular Weight: | 241.53 g./mol | Molecular Formula: | C₁₁H₁₇BClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384268 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. Its boronic acid group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. This makes it essential in the development of drugs, especially those targeting specific biological pathways. Additionally, its cyclopropylamino moiety can contribute to the stability and bioavailability of the final drug product. Researchers also utilize it in the synthesis of bioactive compounds for potential therapeutic applications, including enzyme inhibitors and receptor modulators. Its hydrochloride form ensures better solubility and handling in laboratory settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £1,135.37 |
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(4-(1-(Cyclopropylamino)ethyl)phenyl)boronic acid hydrochloride
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. Its boronic acid group is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. This makes it essential in the development of drugs, especially those targeting specific biological pathways. Additionally, its cyclopropylamino moiety can contribute to the stability and bioavailability of the final drug product. Researchers also utilize it in the synthesis of bioactive compounds for potential therapeutic applications, including enzyme inhibitors and receptor modulators. Its hydrochloride form ensures better solubility and handling in laboratory settings.
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