tert-Butyl 8-methyl-3,8-diazabicyclo[3.2.1]octane-3-carboxylate
95%
- Product Code: 82684
CAS:
1639111-11-7
Molecular Weight: | 226.32 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₂ |
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Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a diazabicyclo[3.2.1]octane core, is particularly valuable in the development of pharmaceutical agents targeting neurological disorders. The compound is often employed in the preparation of ligands for nicotinic acetylcholine receptors, which play a crucial role in cognitive functions and neurotransmission. Additionally, its tert-butyl carboxylate group provides stability and facilitates further chemical modifications, making it a versatile building block in drug discovery. Researchers also explore its potential in creating novel compounds with analgesic or anti-inflammatory properties, leveraging its unique bicyclic framework to enhance binding affinity and selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,750.00 |
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0.250 | 10-20 days | ฿12,600.00 |
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1.000 | 10-20 days | ฿23,625.00 |
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tert-Butyl 8-methyl-3,8-diazabicyclo[3.2.1]octane-3-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a diazabicyclo[3.2.1]octane core, is particularly valuable in the development of pharmaceutical agents targeting neurological disorders. The compound is often employed in the preparation of ligands for nicotinic acetylcholine receptors, which play a crucial role in cognitive functions and neurotransmission. Additionally, its tert-butyl carboxylate group provides stability and facilitates further chemical modifications, making it a versatile building block in drug discovery. Researchers also explore its potential in creating novel compounds with analgesic or anti-inflammatory properties, leveraging its unique bicyclic framework to enhance binding affinity and selectivity.
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