1-(tert-Butyl) 4-ethyl 3-oxoazepane-1,4-dicarboxylate
95%
- Product Code: 83085
CAS:
98977-38-9
| Molecular Weight: | 285.34 g./mol | Molecular Formula: | C₁₄H₂₃NO₅ |
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| EC Number: | MDL Number: | MFCD24466182 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the development of pharmaceuticals. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a versatile building block for constructing azepane-based compounds, which are often found in bioactive molecules. The presence of the 3-oxo group further enhances its reactivity, allowing for various functionalization reactions. It is commonly employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for their potential therapeutic applications. Additionally, its stability and reactivity make it suitable for use in multi-step synthetic routes, particularly in the production of compounds targeting neurological disorders or other medical conditions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $705.17 |
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| 0.250 | 10-20 days | $1,410.35 |
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1-(tert-Butyl) 4-ethyl 3-oxoazepane-1,4-dicarboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the development of pharmaceuticals. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a versatile building block for constructing azepane-based compounds, which are often found in bioactive molecules. The presence of the 3-oxo group further enhances its reactivity, allowing for various functionalization reactions. It is commonly employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for their potential therapeutic applications. Additionally, its stability and reactivity make it suitable for use in multi-step synthetic routes, particularly in the production of compounds targeting neurological disorders or other medical conditions.
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