TERT-BUTYL 4-HYDROXY-3-METHYLAZEPANE-1-CARBOXYLATE
95%
- Product Code: 119579
CAS:
1823857-10-8
| Molecular Weight: | 229.32 g./mol | Molecular Formula: | C₁₂H₂₃NO₃ |
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| EC Number: | MDL Number: | MFCD28119180 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure is particularly valuable in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic effects. Researchers often employ it in the creation of novel drugs targeting neurological disorders, as its azepane ring can mimic certain biological structures, enhancing drug efficacy. Additionally, it finds use in the preparation of chiral ligands for asymmetric catalysis, aiding in the production of enantiomerically pure substances critical in fine chemical and pharmaceutical industries. Its stability and reactivity make it a versatile building block in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $552.14 |
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| 0.250 | 10-20 days | $976.86 |
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TERT-BUTYL 4-HYDROXY-3-METHYLAZEPANE-1-CARBOXYLATE
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure is particularly valuable in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic effects. Researchers often employ it in the creation of novel drugs targeting neurological disorders, as its azepane ring can mimic certain biological structures, enhancing drug efficacy. Additionally, it finds use in the preparation of chiral ligands for asymmetric catalysis, aiding in the production of enantiomerically pure substances critical in fine chemical and pharmaceutical industries. Its stability and reactivity make it a versatile building block in medicinal chemistry and drug discovery processes.
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