RAcemic-(3S,3aS,6aS)-5-(tert-butoxycarbonyl)hexahydro-2H-furo[2,3-c]pyrrole-3-carboxylic acid
95%
- Product Code: 87921
CAS:
1273566-32-7
| Molecular Weight: | 257.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₅ |
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| EC Number: | MDL Number: | MFCD18793342 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. Its structure, featuring a fused furo-pyrrole ring system, makes it a valuable intermediate in the construction of biologically active compounds. It is often employed in the preparation of drug candidates targeting various therapeutic areas, including central nervous system disorders and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions at other functional sites. Additionally, its chiral centers enable its use in stereoselective synthesis, contributing to the production of enantiomerically pure substances.
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-(3S,3aS,6aS)-5-(tert-butoxycarbonyl)hexahydro-2H-furo[2,3-c]pyrrole-3-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. Its structure, featuring a fused furo-pyrrole ring system, makes it a valuable intermediate in the construction of biologically active compounds. It is often employed in the preparation of drug candidates targeting various therapeutic areas, including central nervous system disorders and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, allowing for selective reactions at other functional sites. Additionally, its chiral centers enable its use in stereoselective synthesis, contributing to the production of enantiomerically pure substances.
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