2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-8-thia-2-azaspiro[4.5]decane-4-carboxylic acid 8,8-dioxide
95%
- Product Code: 115561
CAS:
1823835-45-5
| Molecular Weight: | 455.52 g./mol | Molecular Formula: | C₂₄H₂₅NO₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28119059 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for carboxylic acids. Its structure allows it to stabilize sensitive intermediates during the synthesis process, ensuring that the desired peptide sequence is achieved without unwanted side reactions. Additionally, its unique spirocyclic and thia-aza features make it suitable for applications in medicinal chemistry, where it can be incorporated into drug candidates to enhance their stability or bioavailability. The compound is also valuable in research for developing novel organic molecules with potential therapeutic properties. Its ability to act as a protective group while maintaining compatibility with various reaction conditions makes it a versatile tool in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft157,862.23 |
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| 0.100 | 10-20 days | Ft378,171.19 |
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2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-8-thia-2-azaspiro[4.5]decane-4-carboxylic acid 8,8-dioxide
This chemical is primarily used in peptide synthesis as a protecting group for carboxylic acids. Its structure allows it to stabilize sensitive intermediates during the synthesis process, ensuring that the desired peptide sequence is achieved without unwanted side reactions. Additionally, its unique spirocyclic and thia-aza features make it suitable for applications in medicinal chemistry, where it can be incorporated into drug candidates to enhance their stability or bioavailability. The compound is also valuable in research for developing novel organic molecules with potential therapeutic properties. Its ability to act as a protective group while maintaining compatibility with various reaction conditions makes it a versatile tool in synthetic organic chemistry.
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