Racemic-(3aR,4R,6aS)-tert-butyl 4-(aminomethyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
95%
- Product Code: 87821
CAS:
1251012-52-8
| Molecular Weight: | 240.35 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₂ |
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| EC Number: | MDL Number: | MFCD12198694 | |
| 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 more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring both an aminomethyl group and a tert-butyl carbamate moiety, makes it a valuable building block for the development of pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds that interact with biological targets, such as enzymes or receptors, due to its potential to introduce specific functional groups into drug candidates. Additionally, its stereochemistry allows for the exploration of chiral compounds, which is crucial in optimizing the efficacy and selectivity of potential drugs. Overall, it serves as a versatile scaffold in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿3,150.00 |
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| 0.005 | 10-20 days | ฿5,445.00 |
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Racemic-(3aR,4R,6aS)-tert-butyl 4-(aminomethyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those targeting therapeutic applications. Its structure, featuring both an aminomethyl group and a tert-butyl carbamate moiety, makes it a valuable building block for the development of pharmaceutical agents. Researchers often employ it in the design and synthesis of compounds that interact with biological targets, such as enzymes or receptors, due to its potential to introduce specific functional groups into drug candidates. Additionally, its stereochemistry allows for the exploration of chiral compounds, which is crucial in optimizing the efficacy and selectivity of potential drugs. Overall, it serves as a versatile scaffold in drug discovery and development processes.
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