rel-(3aS,4R,7aS)-2-(tert-Butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid
95%
- Product Code: 51166
CAS:
1251021-43-8
| Molecular Weight: | 269.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12198705 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where selective deprotection is required. Additionally, its isoindole scaffold is often explored in the design of inhibitors targeting enzymes or receptors, contributing to drug discovery efforts. The compound’s stereochemistry also allows for the creation of chiral molecules, which are crucial in the production of enantiomerically pure drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €529.25 |
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| 0.250 | 10-20 days | €1,141.13 |
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rel-(3aS,4R,7aS)-2-(tert-Butoxycarbonyl)octahydro-1H-isoindole-4-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where selective deprotection is required. Additionally, its isoindole scaffold is often explored in the design of inhibitors targeting enzymes or receptors, contributing to drug discovery efforts. The compound’s stereochemistry also allows for the creation of chiral molecules, which are crucial in the production of enantiomerically pure drugs.
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