6-Phenyl-2-(3-phenyl-2-aziridinyl)-3-oxa-1-azabicyclo[3.1.0]hexan-4-ol
solid
- Product Code: 50521
CAS:
919101-04-5
| Molecular Weight: | 294.35 g./mol | Molecular Formula: | C₁₈H₁₈N₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 132-136℃ | Boiling Point: | |
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its unique bicyclic structure, incorporating both aziridine and oxa-azabicyclo components, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of antibiotics and other therapeutic agents, particularly those targeting bacterial infections. Additionally, its reactive aziridine ring allows it to participate in ring-opening reactions, which are useful for creating diverse chemical scaffolds. Researchers also explore its potential in asymmetric synthesis due to its chiral centers, enabling the production of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €164.07 |
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6-Phenyl-2-(3-phenyl-2-aziridinyl)-3-oxa-1-azabicyclo[3.1.0]hexan-4-ol
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its unique bicyclic structure, incorporating both aziridine and oxa-azabicyclo components, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of antibiotics and other therapeutic agents, particularly those targeting bacterial infections. Additionally, its reactive aziridine ring allows it to participate in ring-opening reactions, which are useful for creating diverse chemical scaffolds. Researchers also explore its potential in asymmetric synthesis due to its chiral centers, enabling the production of enantiomerically pure substances.
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