(3aS,5R,7aR)-rel-tert-Butyl 5-hydroxyhexahydro-1H-isoindole-2(3H)-carboxylate
98%
- Product Code: 70896
CAS:
2007919-65-3
| Molecular Weight: | 241.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₃ |
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| EC Number: | MDL Number: | MFCD30478085 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a tert-butyl group and a hydroxyl group, makes it a valuable building block for the development of novel compounds. It is often employed in the synthesis of biologically active molecules, such as potential drug candidates, where its stereochemistry and functional groups play a critical role in achieving desired pharmacological properties. Additionally, it can be used in the preparation of chiral ligands or catalysts for asymmetric synthesis, aiding in the creation of enantiomerically pure substances. Its stability and reactivity make it a versatile component in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $130.44 |
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| 1.000 | 10-20 days | $351.71 |
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| 5.000 | 10-20 days | $1,258.08 |
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(3aS,5R,7aR)-rel-tert-Butyl 5-hydroxyhexahydro-1H-isoindole-2(3H)-carboxylate
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a tert-butyl group and a hydroxyl group, makes it a valuable building block for the development of novel compounds. It is often employed in the synthesis of biologically active molecules, such as potential drug candidates, where its stereochemistry and functional groups play a critical role in achieving desired pharmacological properties. Additionally, it can be used in the preparation of chiral ligands or catalysts for asymmetric synthesis, aiding in the creation of enantiomerically pure substances. Its stability and reactivity make it a versatile component in medicinal chemistry and drug discovery processes.
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