tert-Butyl 8-oxo-5-azaspiro[3.5]nonane-5-carboxylate

95%

Reagent Code: #54181
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CAS Number 778646-92-7

science Other reagents with same CAS 778646-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.3107 g/mol
Formula C₁₃H₂₁NO₃
badge Registry Numbers
MDL Number MFCD09336375
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of pharmaceuticals. Its unique spirocyclic structure makes it valuable for constructing complex molecules, often serving as a building block in the synthesis of biologically active compounds. It is commonly employed in the preparation of potential drug candidates, especially those targeting neurological or metabolic disorders. The tert-butyl group provides stability and facilitates specific reactions, making it a versatile reagent in medicinal chemistry research. Additionally, its application extends to the study of enzyme inhibitors and receptor modulators, where its structural features are exploited to enhance binding affinity and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,952.00

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tert-Butyl 8-oxo-5-azaspiro[3.5]nonane-5-carboxylate
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This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the development of pharmaceuticals. Its unique spirocyclic structure makes it valuable for constructing complex molecules, often serving as a building block in the synthesis of biologically active compounds. It is commonly employed in the preparation of potential drug candidates, especially those targeting neurological or metabolic disorders. The tert-butyl group provides stability and facilitates specific reactions, making it a versatile reagent in medicinal chemistry research. Additionally, its application extends to the study of enzyme inhibitors and receptor modulators, where its structural features are exploited to enhance binding affinity and selectivity.
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