(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine
97%
- Product Code: 36236
CAS:
1207276-00-3
| Molecular Weight: | 151.18 g./mol | Molecular Formula: | C₉H₁₀FN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28398056 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine is a compound with potential applications in medicinal chemistry and drug development. Its unique cyclopropane structure, combined with the presence of a fluorophenyl group, makes it a valuable intermediate in the synthesis of biologically active molecules. It is particularly relevant in the design of central nervous system (CNS) drugs, where its structural features may contribute to binding affinity and selectivity for specific receptors or enzymes. The compound's stereochemistry also plays a critical role in its pharmacological activity, making it a candidate for the development of enantioselective drugs. Additionally, its fluorine substituent can enhance metabolic stability and bioavailability, which are key considerations in drug optimization. Researchers may explore its use in creating novel antidepressants, anxiolytics, or other neuropharmacological agents due to its potential interaction with neurotransmitter systems.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $270.03 |
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| 0.250 | 10-20 days | $513.05 |
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(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine
(1S,2R)-2-(4-Fluorophenyl)cyclopropanamine is a compound with potential applications in medicinal chemistry and drug development. Its unique cyclopropane structure, combined with the presence of a fluorophenyl group, makes it a valuable intermediate in the synthesis of biologically active molecules. It is particularly relevant in the design of central nervous system (CNS) drugs, where its structural features may contribute to binding affinity and selectivity for specific receptors or enzymes. The compound's stereochemistry also plays a critical role in its pharmacological activity, making it a candidate for the development of enantioselective drugs. Additionally, its fluorine substituent can enhance metabolic stability and bioavailability, which are key considerations in drug optimization. Researchers may explore its use in creating novel antidepressants, anxiolytics, or other neuropharmacological agents due to its potential interaction with neurotransmitter systems.
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