3,6-Diazaspiro[3.3]heptane-6-carboxylic acid tert-butyl ester hemioxylate
95%
- Product Code: 75408
CAS:
1272412-72-2
| Molecular Weight: | 486.57 g./mol | Molecular Formula: | C₂₂H₃₈N₄O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18782894 | |
| Melting Point: | Boiling Point: | 282.6±15.0℃ at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block or intermediate in the development of more complex molecules. Its spirocyclic structure makes it valuable in the design of pharmaceuticals, where it can contribute to the formation of novel drug candidates with potential therapeutic properties. The tert-butyl ester group enhances its stability, allowing for easier handling and storage during synthetic processes. Additionally, its hemioxylate form may improve solubility, facilitating its use in various reaction conditions. Researchers often employ this compound in the synthesis of bioactive compounds, including those targeting neurological or metabolic disorders, due to its unique structural features that can influence binding affinity and selectivity. Its application extends to the development of agrochemicals and other fine chemicals, where its framework can be incorporated to enhance efficacy or modify physical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿92,510.00 |
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| 0.250 | 10-20 days | ฿199,190.00 |
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3,6-Diazaspiro[3.3]heptane-6-carboxylic acid tert-butyl ester hemioxylate
This chemical is primarily utilized in the field of organic synthesis, particularly as a building block or intermediate in the development of more complex molecules. Its spirocyclic structure makes it valuable in the design of pharmaceuticals, where it can contribute to the formation of novel drug candidates with potential therapeutic properties. The tert-butyl ester group enhances its stability, allowing for easier handling and storage during synthetic processes. Additionally, its hemioxylate form may improve solubility, facilitating its use in various reaction conditions. Researchers often employ this compound in the synthesis of bioactive compounds, including those targeting neurological or metabolic disorders, due to its unique structural features that can influence binding affinity and selectivity. Its application extends to the development of agrochemicals and other fine chemicals, where its framework can be incorporated to enhance efficacy or modify physical properties.
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