tert-Butyl 3-nitropyrrolidine-1-carboxylate

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Reagent Code: #152785
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CAS Number 1309581-43-8

science Other reagents with same CAS 1309581-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.24 g/mol
Formula C₉H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD21337917
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. The nitro group allows for further functionalization, enabling conversion to amines or other nitrogen-containing derivatives, which are common in medicinal chemistry. The tert-butoxycarbonyl (Boc) protecting group stabilizes the nitrogen during multi-step syntheses, making it valuable in the preparation of complex heterocyclic systems. Commonly employed in research settings for constructing pyrrolidine-based scaffolds found in neurological and cardiovascular agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,980.00
inventory 250mg
10-20 days ฿10,300.00
inventory 1g
10-20 days ฿12,870.00
inventory 5g
10-20 days ฿38,770.00

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tert-Butyl 3-nitropyrrolidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. The nitro group allows for further functionalization, enabling conversion to amines or other nitrogen-containing derivatives, which are common in medicinal chemistry. The tert-butoxycarbonyl (Boc) protecting group stabilizes the nitrogen during multi-step syntheses, making it valuable in the preparation of complex heterocyclic systems. Commonly employed in rese

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. The nitro group allows for further functionalization, enabling conversion to amines or other nitrogen-containing derivatives, which are common in medicinal chemistry. The tert-butoxycarbonyl (Boc) protecting group stabilizes the nitrogen during multi-step syntheses, making it valuable in the preparation of complex heterocyclic systems. Commonly employed in research settings for constructing pyrrolidine-based scaffolds found in neurological and cardiovascular agents.

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