2-(3-(tert-Butoxycarbonyl)-3-azabicyclo-[3.2.1]octan-8-yl)acetic acid
95%
- Product Code: 62322
CAS:
1250996-75-8
| Molecular Weight: | 269.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17016675 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of complex pharmaceutical agents. Its structure, featuring a bicyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the development of drugs targeting neurological disorders, as the azabicyclo[3.2.1]octane moiety can mimic certain neurotransmitter structures. Additionally, the Boc group allows for selective deprotection during multi-step synthesis, enabling precise modifications to the molecule. This chemical is also explored in the creation of peptidomimetics, which are used to inhibit protein-protein interactions in therapeutic applications. Its versatility makes it a key component in the design of novel bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,431.00 |
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| 0.250 | 10-20 days | ฿17,235.00 |
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2-(3-(tert-Butoxycarbonyl)-3-azabicyclo-[3.2.1]octan-8-yl)acetic acid
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of complex pharmaceutical agents. Its structure, featuring a bicyclic system and a tert-butoxycarbonyl (Boc) protecting group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the development of drugs targeting neurological disorders, as the azabicyclo[3.2.1]octane moiety can mimic certain neurotransmitter structures. Additionally, the Boc group allows for selective deprotection during multi-step synthesis, enabling precise modifications to the molecule. This chemical is also explored in the creation of peptidomimetics, which are used to inhibit protein-protein interactions in therapeutic applications. Its versatility makes it a key component in the design of novel bioactive compounds.
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