tert-Butyl (3-aminobicyclo[1.1.1]pentan-1-yl)carbamate
97%
- Product Code: 113207
CAS:
1638767-25-5
| Molecular Weight: | 198.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₂ |
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| EC Number: | MDL Number: | MFCD27987307 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its unique bicyclic structure makes it a valuable building block for creating complex molecules, especially in the design of drugs targeting specific biological pathways. The tert-butyl group provides stability and protection for the amine functionality during synthetic processes, enabling selective reactions. It is often employed in the synthesis of peptidomimetics and other bioactive molecules, where its rigid bicyclo[1.1.1]pentane scaffold can mimic natural peptide structures while enhancing metabolic stability and bioavailability. Additionally, it finds use in research focused on developing novel therapeutics for neurological disorders and cancer, owing to its ability to interact with specific protein targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿396.00 |
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| 0.250 | 10-20 days | ฿810.00 |
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| 1.000 | 10-20 days | ฿2,331.00 |
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| 5.000 | 10-20 days | ฿11,133.00 |
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tert-Butyl (3-aminobicyclo[1.1.1]pentan-1-yl)carbamate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its unique bicyclic structure makes it a valuable building block for creating complex molecules, especially in the design of drugs targeting specific biological pathways. The tert-butyl group provides stability and protection for the amine functionality during synthetic processes, enabling selective reactions. It is often employed in the synthesis of peptidomimetics and other bioactive molecules, where its rigid bicyclo[1.1.1]pentane scaffold can mimic natural peptide structures while enhancing metabolic stability and bioavailability. Additionally, it finds use in research focused on developing novel therapeutics for neurological disorders and cancer, owing to its ability to interact with specific protein targets.
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