tert-Butyl 1-benzyl-3-iodo-1,8-diazaspiro[4.5]decane-8-carboxylate
95%
- Product Code: 123910
CAS:
2177264-11-6
| Molecular Weight: | 456.36 g./mol | Molecular Formula: | C₂₀H₂₉IN₂O₂ |
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| EC Number: | MDL Number: | MFCD28390464 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of complex spirocyclic compounds. Its structure, featuring both an iodine atom and a benzyl group, makes it a valuable building block in the development of pharmaceuticals, particularly in the synthesis of bioactive molecules targeting neurological disorders. The iodine moiety allows for further functionalization through cross-coupling reactions, while the spirocyclic framework is often explored for its potential in drug design due to its conformational rigidity and ability to mimic natural structures. Additionally, it serves as a precursor in the synthesis of ligands for catalytic systems, contributing to advancements in asymmetric catalysis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | ฿14,040.00 |
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| 0.250 | 10-20 days | ฿25,443.00 |
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tert-Butyl 1-benzyl-3-iodo-1,8-diazaspiro[4.5]decane-8-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of complex spirocyclic compounds. Its structure, featuring both an iodine atom and a benzyl group, makes it a valuable building block in the development of pharmaceuticals, particularly in the synthesis of bioactive molecules targeting neurological disorders. The iodine moiety allows for further functionalization through cross-coupling reactions, while the spirocyclic framework is often explored for its potential in drug design due to its conformational rigidity and ability to mimic natural structures. Additionally, it serves as a precursor in the synthesis of ligands for catalytic systems, contributing to advancements in asymmetric catalysis.
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