(S)-tert-Butyl 3-((6-(cyclopropylamino)pyrimidin-4-yl)amino)pyrrolidine-1-carboxylate

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Reagent Code: #232423
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CAS Number 1353994-21-4

science Other reagents with same CAS 1353994-21-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.4 g/mol
Formula C₁₆H₂₅N₅O₂
thermostat Physical Properties
Boiling Point 511.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.292±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in constructing protease or NS5A inhibitors. The compound's chiral center and protected amine group allow for controlled coupling reactions in multi-step drug synthesis. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties of new drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,720.00
inventory 1g
10-20 days ฿44,470.00
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(S)-tert-Butyl 3-((6-(cyclopropylamino)pyrimidin-4-yl)amino)pyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in constructing protease or NS5A inhibitors. The compound's chiral center and protected amine group allow for controlled coupling reactions in multi-step drug synthesis. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties of new drug candidates.

Used as a key intermediate in the synthesis of antiviral agents, particularly in the development of hepatitis C virus (HCV) inhibitors. Its structure enables selective binding to viral enzymes, making it valuable in constructing protease or NS5A inhibitors. The compound's chiral center and protected amine group allow for controlled coupling reactions in multi-step drug synthesis. It is also employed in medicinal chemistry research to optimize pharmacokinetic properties of new drug candidates.

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