(3AR,8aS)-2-(5-(trifluoromethyl)pyridin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole
98%,99%ee
- Product Code: 55647
CAS:
2097333-76-9
| Molecular Weight: | 304.2600 g./mol | Molecular Formula: | C₁₆H₁₁F₃N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31706429 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block in the synthesis of more complex molecules. Its structure, featuring a trifluoromethylpyridine moiety and an indenoxazole core, makes it particularly valuable in the development of pharmaceuticals targeting specific biological pathways. It is often explored for its potential in creating drugs that interact with enzymes or receptors, particularly in the treatment of diseases such as cancer, inflammation, or neurological disorders. Additionally, its unique chemical framework allows for further modifications, enabling researchers to fine-tune the compound's properties for enhanced efficacy and selectivity in drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,411.00 |
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(3AR,8aS)-2-(5-(trifluoromethyl)pyridin-2-yl)-3a,8a-dihydro-8H-indeno[1,2-d]oxazole
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block in the synthesis of more complex molecules. Its structure, featuring a trifluoromethylpyridine moiety and an indenoxazole core, makes it particularly valuable in the development of pharmaceuticals targeting specific biological pathways. It is often explored for its potential in creating drugs that interact with enzymes or receptors, particularly in the treatment of diseases such as cancer, inflammation, or neurological disorders. Additionally, its unique chemical framework allows for further modifications, enabling researchers to fine-tune the compound's properties for enhanced efficacy and selectivity in drug discovery programs.
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