5-Oxa-7-azaspiro[3.4]octan-6-one
95%
- Product Code: 66044
CAS:
27784-33-4
| Molecular Weight: | 127.14 g./mol | Molecular Formula: | C₆H₉NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19221829 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of complex molecules. Its unique spirocyclic structure makes it particularly useful in the construction of heterocyclic compounds, which are often found in pharmaceuticals and agrochemicals. Researchers leverage its reactivity to introduce specific functional groups or to create novel ring systems, enabling the design of new drugs or biologically active compounds. Additionally, it may be employed in material science for the synthesis of specialized polymers or coatings, where its structural properties can impart desired characteristics such as stability or flexibility. Its application is also explored in the development of catalysts or ligands for asymmetric synthesis, contributing to advancements in stereoselective reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿264,380.00 |
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5-Oxa-7-azaspiro[3.4]octan-6-one
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of complex molecules. Its unique spirocyclic structure makes it particularly useful in the construction of heterocyclic compounds, which are often found in pharmaceuticals and agrochemicals. Researchers leverage its reactivity to introduce specific functional groups or to create novel ring systems, enabling the design of new drugs or biologically active compounds. Additionally, it may be employed in material science for the synthesis of specialized polymers or coatings, where its structural properties can impart desired characteristics such as stability or flexibility. Its application is also explored in the development of catalysts or ligands for asymmetric synthesis, contributing to advancements in stereoselective reactions.
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