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
EC Number: MDL Number:
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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
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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