(1S,4R)-2-Azabicyclo[2.2.1]hept-5-en-3-one
97%
- Product Code: 73945
CAS:
130931-83-8
| Molecular Weight: | 109.13 g./mol | Molecular Formula: | C₆H₇NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00211275 | |
| Melting Point: | 92-100°C | Boiling Point: | 319.302°C at 760 mmHg |
| Density: | 1.199g/cm3 | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of chiral intermediates for drug production. Its unique bicyclic structure makes it valuable in creating molecules with specific stereochemistry, which is crucial for the efficacy and safety of many drugs. It is often employed in the preparation of antiviral and antibacterial agents, where precise molecular configuration is essential. Additionally, it serves as a key building block in organic synthesis, enabling the construction of complex frameworks used in medicinal chemistry and research. Its role in facilitating enantioselective reactions further enhances its importance in producing high-purity active pharmaceutical ingredients (APIs).
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-White solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿480.00 |
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| 0.250 | 10-20 days | ฿340.00 |
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| 1.000 | 10-20 days | ฿1,350.00 |
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| 5.000 | 10-20 days | ฿6,500.00 |
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(1S,4R)-2-Azabicyclo[2.2.1]hept-5-en-3-one
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of chiral intermediates for drug production. Its unique bicyclic structure makes it valuable in creating molecules with specific stereochemistry, which is crucial for the efficacy and safety of many drugs. It is often employed in the preparation of antiviral and antibacterial agents, where precise molecular configuration is essential. Additionally, it serves as a key building block in organic synthesis, enabling the construction of complex frameworks used in medicinal chemistry and research. Its role in facilitating enantioselective reactions further enhances its importance in producing high-purity active pharmaceutical ingredients (APIs).
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