tert-Butyl 8-oxo-5-thia-2-azaspiro[3.4]octane-2-carboxylate 5,5-dioxide

Reagent Code: #149559
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CAS Number 1340481-91-5

science Other reagents with same CAS 1340481-91-5

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scatter_plot Molecular Information
Weight 275.32 g/mol
Formula C₁₁H₁₇NO₅S
badge Registry Numbers
MDL Number MFCD22370065
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cysteine protease inhibitors. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with biological activity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory diseases and certain viral infections. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, enhancing selectivity and yield in peptide-like frameworks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿59,800.00

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tert-Butyl 8-oxo-5-thia-2-azaspiro[3.4]octane-2-carboxylate 5,5-dioxide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cysteine protease inhibitors. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with biological activity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory diseases and certain viral infections. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, enhancing s

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of cysteine protease inhibitors. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with biological activity. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory diseases and certain viral infections. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, enhancing selectivity and yield in peptide-like frameworks.

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