(4aS,7aS)-6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridine
95%
- Product Code: 69782
CAS:
151213-39-7
| Molecular Weight: | 216.32 g./mol | Molecular Formula: | C₁₄H₂₀N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06796543 | |
| Melting Point: | Boiling Point: | 385.4 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a benzyl group and a fused bicyclic system, makes it a valuable building block for developing compounds with potential therapeutic effects. Specifically, it is often employed in the design and synthesis of drugs targeting the central nervous system, such as antidepressants, anxiolytics, and antipsychotics. Additionally, its unique stereochemistry and functional groups allow for further chemical modifications, enabling researchers to explore its applications in creating novel bioactive molecules with improved efficacy and selectivity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to brown Liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿2,900.00 |
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| 0.050 | 10-20 days | ฿8,800.00 |
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| 0.100 | 10-20 days | ฿13,600.00 |
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| 0.250 | 10-20 days | ฿32,000.00 |
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(4aS,7aS)-6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a benzyl group and a fused bicyclic system, makes it a valuable building block for developing compounds with potential therapeutic effects. Specifically, it is often employed in the design and synthesis of drugs targeting the central nervous system, such as antidepressants, anxiolytics, and antipsychotics. Additionally, its unique stereochemistry and functional groups allow for further chemical modifications, enabling researchers to explore its applications in creating novel bioactive molecules with improved efficacy and selectivity.
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