(S,S)-2,8-Diazabicyclo[4,3,0]nonane
99%
- Product Code: 71415
CAS:
151213-42-2
| Molecular Weight: | 126.2 g./mol | Molecular Formula: | C₇H₁₄N₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is employed in the preparation of pharmaceuticals to ensure the production of specific enantiomers, which can significantly impact the efficacy and safety of drugs. Additionally, it serves as a building block in organic synthesis for creating complex molecular structures with high precision. Its bicyclic structure and stereochemistry make it valuable in designing catalysts for various chemical transformations, including hydrogenation and carbon-carbon bond formation.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale -yellow Liquid |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $63.28 |
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| 5.000 | 10-20 days | $137.12 |
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| 25.000 | 10-20 days | $450.02 |
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| 100.000 | 10-20 days | $1,350.07 |
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(S,S)-2,8-Diazabicyclo[4,3,0]nonane
Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is employed in the preparation of pharmaceuticals to ensure the production of specific enantiomers, which can significantly impact the efficacy and safety of drugs. Additionally, it serves as a building block in organic synthesis for creating complex molecular structures with high precision. Its bicyclic structure and stereochemistry make it valuable in designing catalysts for various chemical transformations, including hydrogenation and carbon-carbon bond formation.
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