8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carbaldehyde
99%
- Product Code: 75784
CAS:
56327-24-3
| Molecular Weight: | 246 g./mol | Molecular Formula: | C₁₅H₁₈O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26399860 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. The aldehyde group present in the molecule allows for further functionalization through reactions such as oxidation, reduction, or condensation, enabling the creation of diverse chemical entities. Additionally, it finds application in material science, where it can be used to design novel polymers or coatings with specific properties. Its role in the synthesis of chiral compounds is also noteworthy, as the spirocyclic framework can influence stereochemistry in asymmetric synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿85,500.00 |
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| 1.000 | 10-20 days | ฿124,690.00 |
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8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carbaldehyde
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. Its unique spirocyclic structure makes it valuable in the development of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. The aldehyde group present in the molecule allows for further functionalization through reactions such as oxidation, reduction, or condensation, enabling the creation of diverse chemical entities. Additionally, it finds application in material science, where it can be used to design novel polymers or coatings with specific properties. Its role in the synthesis of chiral compounds is also noteworthy, as the spirocyclic framework can influence stereochemistry in asymmetric synthesis.
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