(4S,4'S)-2,2'-Cyclopentylidenebis[4,5-dihydro-4-(phenylmethyl)oxazole]
≥95%
- Product Code: 59742
CAS:
1003886-05-2
| Molecular Weight: | 388.5 g./mol | Molecular Formula: | C₂₅H₂₈N₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 524.0±33.0 °C | |
| Density: | 1.21±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral catalysts. Its unique structure, featuring a cyclopentylidene bridge and oxazole rings, makes it highly effective in facilitating enantioselective reactions. These reactions are crucial in the production of pharmaceuticals, where the chirality of molecules often determines their biological activity and efficacy.
Additionally, it is employed in organic synthesis to construct complex molecular frameworks with high precision. Its ability to induce stereocontrol in chemical transformations is valuable in the synthesis of fine chemicals and intermediates. Researchers also explore its potential in materials science, where chiral molecules can influence the properties of advanced materials. Overall, its applications are centered around enhancing selectivity and efficiency in chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,499.00 |
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(4S,4'S)-2,2'-Cyclopentylidenebis[4,5-dihydro-4-(phenylmethyl)oxazole]
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral catalysts. Its unique structure, featuring a cyclopentylidene bridge and oxazole rings, makes it highly effective in facilitating enantioselective reactions. These reactions are crucial in the production of pharmaceuticals, where the chirality of molecules often determines their biological activity and efficacy.
Additionally, it is employed in organic synthesis to construct complex molecular frameworks with high precision. Its ability to induce stereocontrol in chemical transformations is valuable in the synthesis of fine chemicals and intermediates. Researchers also explore its potential in materials science, where chiral molecules can influence the properties of advanced materials. Overall, its applications are centered around enhancing selectivity and efficiency in chemical processes.
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