RAcemic-(3aR,5R,7aR)-tert-butyl 5-(hydroxymethyl)hexahydropyrano[3,2-b]pyrrole-1(2H)-carboxylate
95%
- Product Code: 87079
CAS:
1310381-38-4
| Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
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| EC Number: | MDL Number: | MFCD21362257 | |
| 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, particularly as an intermediate in the production of more complex molecules. Its structure, featuring a hexahydropyrano[3,2-b]pyrrole core, makes it valuable for constructing biologically active compounds, such as pharmaceuticals or agrochemicals. The presence of the tert-butyl group and hydroxymethyl functionality allows for further chemical modifications, enabling the creation of diverse derivatives. It is often employed in medicinal chemistry research to develop potential drug candidates, especially in the synthesis of molecules targeting specific enzymes or receptors. Additionally, its stereochemistry plays a crucial role in the design of chiral compounds, which are essential for achieving desired biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $776.33 |
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RAcemic-(3aR,5R,7aR)-tert-butyl 5-(hydroxymethyl)hexahydropyrano[3,2-b]pyrrole-1(2H)-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. Its structure, featuring a hexahydropyrano[3,2-b]pyrrole core, makes it valuable for constructing biologically active compounds, such as pharmaceuticals or agrochemicals. The presence of the tert-butyl group and hydroxymethyl functionality allows for further chemical modifications, enabling the creation of diverse derivatives. It is often employed in medicinal chemistry research to develop potential drug candidates, especially in the synthesis of molecules targeting specific enzymes or receptors. Additionally, its stereochemistry plays a crucial role in the design of chiral compounds, which are essential for achieving desired biological activity.
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