tert-Butyl 6-carboxy-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate
95%
- Product Code: 75735
CAS:
921760-85-2
| Molecular Weight: | 361.39 g./mol | Molecular Formula: | C₁₉H₂₃NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11501220 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting therapeutic areas such as central nervous system disorders and inflammation. Its structural features, including the spirocyclic system and functional groups, make it a valuable building block for designing molecules with potential drug-like properties. Researchers often employ it in medicinal chemistry to explore and optimize lead compounds, aiming to enhance efficacy, selectivity, and pharmacokinetic profiles. Additionally, it may be used in the preparation of analogs for structure-activity relationship (SAR) studies, contributing to the discovery of novel therapeutics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿122,930.00 |
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| 5.000 | 10-20 days | ฿429,790.00 |
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tert-Butyl 6-carboxy-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting therapeutic areas such as central nervous system disorders and inflammation. Its structural features, including the spirocyclic system and functional groups, make it a valuable building block for designing molecules with potential drug-like properties. Researchers often employ it in medicinal chemistry to explore and optimize lead compounds, aiming to enhance efficacy, selectivity, and pharmacokinetic profiles. Additionally, it may be used in the preparation of analogs for structure-activity relationship (SAR) studies, contributing to the discovery of novel therapeutics.
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