endo-9-Boc-7-hydroxy-3-oxa-9-azabicyclo[3.3.1]nonane
≥95%
- Product Code: 71294
CAS:
1148006-31-8
| Molecular Weight: | 243.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27956889 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and cardiovascular diseases. The Boc (tert-butoxycarbonyl) protecting group in the structure is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Its bicyclic framework is often exploited in the design of drugs that require rigid, three-dimensional structures to interact effectively with biological targets. Additionally, the hydroxyl group provides a site for further functionalization, enabling the attachment of various pharmacophores to enhance drug efficacy or modify pharmacokinetic properties. This chemical is particularly valuable in medicinal chemistry for constructing nitrogen-containing heterocycles, which are prevalent in many therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $953.09 |
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endo-9-Boc-7-hydroxy-3-oxa-9-azabicyclo[3.3.1]nonane
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those targeting neurological and cardiovascular diseases. The Boc (tert-butoxycarbonyl) protecting group in the structure is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Its bicyclic framework is often exploited in the design of drugs that require rigid, three-dimensional structures to interact effectively with biological targets. Additionally, the hydroxyl group provides a site for further functionalization, enabling the attachment of various pharmacophores to enhance drug efficacy or modify pharmacokinetic properties. This chemical is particularly valuable in medicinal chemistry for constructing nitrogen-containing heterocycles, which are prevalent in many therapeutic agents.
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