RAcemic-(4aS,6R,7aS)-4-tert-butyl 6-ethyl hexahydrocyclopenta[b][1,4]oxazine-4,6(4aH)-dicarboxylate
95%
- Product Code: 87110
CAS:
1290627-68-7
| Molecular Weight: | 299.36 g./mol | Molecular Formula: | C₁₅H₂₅NO₅ |
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| EC Number: | MDL Number: | MFCD19442507 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring a cyclopenta[b][1,4]oxazine core, makes it valuable for constructing biologically active compounds, particularly in pharmaceutical research. It is often employed in the development of chiral molecules, leveraging its stereochemistry to influence the enantioselectivity of reactions. Additionally, this chemical finds application in the study of heterocyclic chemistry, aiding in the exploration of novel reaction pathways and the synthesis of new drug candidates. Its tert-butyl and ethyl groups contribute to its stability and reactivity, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿25,875.00 |
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| 0.250 | 10-20 days | ฿50,193.00 |
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RAcemic-(4aS,6R,7aS)-4-tert-butyl 6-ethyl hexahydrocyclopenta[b][1,4]oxazine-4,6(4aH)-dicarboxylate
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its unique structure, featuring a cyclopenta[b][1,4]oxazine core, makes it valuable for constructing biologically active compounds, particularly in pharmaceutical research. It is often employed in the development of chiral molecules, leveraging its stereochemistry to influence the enantioselectivity of reactions. Additionally, this chemical finds application in the study of heterocyclic chemistry, aiding in the exploration of novel reaction pathways and the synthesis of new drug candidates. Its tert-butyl and ethyl groups contribute to its stability and reactivity, making it a versatile building block in medicinal chemistry.
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