tert-Butyl 2,7-diazaspiro[4.5]decane-2-carboxylate
95%
- Product Code: 76003
CAS:
885268-42-8
Molecular Weight: | 240.35 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₂ |
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EC Number: | MDL Number: | MFCD08234437 | |
Melting Point: | Boiling Point: | 337℃ at 760 mmHg | |
Density: | 1.07g/ml | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex molecules. Its unique spirocyclic structure makes it particularly useful in the design and synthesis of pharmaceuticals, especially those targeting neurological and psychiatric disorders. Researchers often employ it to create compounds with potential therapeutic effects, such as inhibitors for specific enzymes or receptors in the brain. Additionally, its stability and reactivity make it a suitable candidate for use in medicinal chemistry projects aimed at discovering new drugs. The compound’s versatility also extends to its role in the synthesis of ligands for biological studies, helping to elucidate mechanisms of action in various biochemical pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,500.00 |
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0.250 | 10-20 days | ฿7,000.00 |
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1.000 | 10-20 days | ฿19,380.00 |
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tert-Butyl 2,7-diazaspiro[4.5]decane-2-carboxylate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a valuable intermediate for the development of more complex molecules. Its unique spirocyclic structure makes it particularly useful in the design and synthesis of pharmaceuticals, especially those targeting neurological and psychiatric disorders. Researchers often employ it to create compounds with potential therapeutic effects, such as inhibitors for specific enzymes or receptors in the brain. Additionally, its stability and reactivity make it a suitable candidate for use in medicinal chemistry projects aimed at discovering new drugs. The compound’s versatility also extends to its role in the synthesis of ligands for biological studies, helping to elucidate mechanisms of action in various biochemical pathways.
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