RAcemic-(3R,3aS,6aS)-5-(tert-butoxycarbonyl)hexahydro-2H-furo[2,3-c]pyrrole-3-carboxylic acid
95%
- Product Code: 87082
CAS:
1273566-11-2
| Molecular Weight: | 257.29 g./mol | Molecular Formula: | C₁₂H₁₉NO₅ |
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| EC Number: | MDL Number: | MFCD18793343 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a furo[2,3-c]pyrrole core and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. It is often employed in peptide chemistry and medicinal chemistry to develop compounds targeting diseases such as cancer, inflammation, and neurological disorders. Additionally, its chiral centers and functional groups allow for further chemical modifications, enabling the creation of diverse molecular libraries for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿26,325.00 |
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| 0.250 | 10-20 days | ฿49,140.00 |
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RAcemic-(3R,3aS,6aS)-5-(tert-butoxycarbonyl)hexahydro-2H-furo[2,3-c]pyrrole-3-carboxylic acid
This compound is primarily used in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various biologically active compounds, including potential drug candidates. Its structure, featuring a furo[2,3-c]pyrrole core and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing molecules with specific stereochemistry and functional groups. It is often employed in peptide chemistry and medicinal chemistry to develop compounds targeting diseases such as cancer, inflammation, and neurological disorders. Additionally, its chiral centers and functional groups allow for further chemical modifications, enabling the creation of diverse molecular libraries for drug discovery.
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