tert-Butyl 3-cyano-3-((trimethylsilyl)oxy)pyrrolidine-1-carboxylate

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Reagent Code: #146541
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CAS Number 942190-60-5

science Other reagents with same CAS 942190-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.43 g/mol
Formula C₁₃H₂₄N₂O₃Si
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules containing pyrrolidine scaffolds. The cyano and silyloxy functional groups allow for further chemical transformations, enabling the introduction of diverse substituents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen atom, making it valuable in multi-step organic syntheses where selective reactivity is required. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing heterocycles.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,150.00
inventory 100mg
10-20 days ฿2,270.00

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tert-Butyl 3-cyano-3-((trimethylsilyl)oxy)pyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules containing pyrrolidine scaffolds. The cyano and silyloxy functional groups allow for further chemical transformations, enabling the introduction of diverse substituents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen atom, making it valuable in multi-step organic syntheses where selective reactivity is required. Commonly employed in medicinal

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules containing pyrrolidine scaffolds. The cyano and silyloxy functional groups allow for further chemical transformations, enabling the introduction of diverse substituents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen atom, making it valuable in multi-step organic syntheses where selective reactivity is required. Commonly employed in medicinal chemistry for constructing complex nitrogen-containing heterocycles.

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