1,8-Diazaspiro[5.5]undecane-8-carboxylicacid tert-butyl ester
95%
- Product Code: 74903
CAS:
1086394-59-3
Molecular Weight: | 254.38 g./mol | Molecular Formula: | C₁₄H₂₆N₂O₂ |
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EC Number: | MDL Number: | MFCD11223538 | |
Melting Point: | Boiling Point: | 354.1±15.0℃ at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, sealed |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate or building block. Its spirocyclic structure makes it valuable in the development of complex molecules, particularly in the design of drugs targeting neurological or metabolic disorders. The tert-butyl ester group enhances its stability, allowing for easier handling and manipulation in synthetic processes. It is often employed in the synthesis of bioactive compounds, including potential therapeutic agents, due to its ability to introduce specific structural motifs that can influence biological activity. Additionally, it may be used in the preparation of ligands for catalysis or in the study of chemical reactions involving spirocyclic frameworks.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿19,160.00 |
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0.500 | 10-20 days | ฿35,680.00 |
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1,8-Diazaspiro[5.5]undecane-8-carboxylicacid tert-butyl ester
This compound is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate or building block. Its spirocyclic structure makes it valuable in the development of complex molecules, particularly in the design of drugs targeting neurological or metabolic disorders. The tert-butyl ester group enhances its stability, allowing for easier handling and manipulation in synthetic processes. It is often employed in the synthesis of bioactive compounds, including potential therapeutic agents, due to its ability to introduce specific structural motifs that can influence biological activity. Additionally, it may be used in the preparation of ligands for catalysis or in the study of chemical reactions involving spirocyclic frameworks.
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