(3aR,4R,7aS)-tert-Butyl 4-aminohexahydro-1H-isoindole-2(3H)-carboxylate
95%
- Product Code: 87823
CAS:
1251001-17-8
| Molecular Weight: | 240.34 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09753917 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical agents. Its structure, featuring a tert-butyl carbamate group and an amino function, makes it a valuable building block for the development of peptidomimetics and other bioactive molecules. It is often employed in the synthesis of compounds targeting neurological disorders, as its isoindoline core can mimic certain peptide structures involved in neurotransmission. Additionally, its chiral centers allow for the creation of enantiomerically pure products, which is crucial in drug development to ensure specificity and reduce side effects. The compound’s stability and reactivity also make it suitable for use in solid-phase peptide synthesis, facilitating the creation of peptide-based therapeutics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿25,857.00 |
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| 0.250 | 10-20 days | ฿50,193.00 |
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(3aR,4R,7aS)-tert-Butyl 4-aminohexahydro-1H-isoindole-2(3H)-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical agents. Its structure, featuring a tert-butyl carbamate group and an amino function, makes it a valuable building block for the development of peptidomimetics and other bioactive molecules. It is often employed in the synthesis of compounds targeting neurological disorders, as its isoindoline core can mimic certain peptide structures involved in neurotransmission. Additionally, its chiral centers allow for the creation of enantiomerically pure products, which is crucial in drug development to ensure specificity and reduce side effects. The compound’s stability and reactivity also make it suitable for use in solid-phase peptide synthesis, facilitating the creation of peptide-based therapeutics.
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