1-(3-bromophenyl)cyclopropan-1-amine hydrochloride
97%
- Product Code: 64494
CAS:
597563-15-0
| Molecular Weight: | 248.55 g./mol | Molecular Formula: | C₉H₁₁BrClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11616353 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in pharmaceutical research to create potential drug candidates, particularly in the synthesis of compounds targeting neurological disorders. The cyclopropane ring and amine group in its structure make it a versatile intermediate for constructing bioactive molecules. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of therapeutic agents. Its bromophenyl moiety also allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿9,280.00 |
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| 5.000 | 10-20 days | ฿28,480.00 |
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| 10.000 | 10-20 days | ฿55,560.00 |
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1-(3-bromophenyl)cyclopropan-1-amine hydrochloride
This compound is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in pharmaceutical research to create potential drug candidates, particularly in the synthesis of compounds targeting neurological disorders. The cyclopropane ring and amine group in its structure make it a versatile intermediate for constructing bioactive molecules. Additionally, it is used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of therapeutic agents. Its bromophenyl moiety also allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
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