2H-Isoindole-2-carboxylic acid, 4-fluoro-1,3-dihydro-, (3R,5S)-5-[[[(1R,2S)-1-[[(cyclopropylsulfonyl)amino]carbonyl]-2-ethenylcyclopropyl]amino]carbonyl]-1-[(1,1-dimethylethoxy)carbonyl]-3-pyrrolidinyl ester

≥95%

Reagent Code: #196144
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CAS Number 905994-07-2

science Other reagents with same CAS 905994-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 606.66 g/mol
Formula C₂₈H₃₅FN₄O₈S
inventory_2 Storage & Handling
Density 1.43±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Shows relevance in antiviral drug research, especially for hepatitis C virus (HCV) treatment. The compound's structure allows for high selectivity and potency in targeting specific enzymes involved in viral replication. Its ester and sulfonamide functional groups enhance bioavailability and metabolic stability in drug formulations. Commonly employed in late-stage synthesis due to its chiral centers and functional group compatibility with peptide-like frameworks.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,930.00
inventory 25mg
10-20 days ฿32,680.00

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2H-Isoindole-2-carboxylic acid, 4-fluoro-1,3-dihydro-, (3R,5S)-5-[[[(1R,2S)-1-[[(cyclopropylsulfonyl)amino]carbonyl]-2-ethenylcyclopropyl]amino]carbonyl]-1-[(1,1-dimethylethoxy)carbonyl]-3-pyrrolidinyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Shows relevance in antiviral drug research, especially for hepatitis C virus (HCV) treatment. The compound's structure allows for high selectivity and potency in targeting specific enzymes involved in viral replication. Its ester and sulfonamide functional groups enhance bioavailability and metabolic stability in drug formulations. Commonly employed in late-stage synthesis due to

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Shows relevance in antiviral drug research, especially for hepatitis C virus (HCV) treatment. The compound's structure allows for high selectivity and potency in targeting specific enzymes involved in viral replication. Its ester and sulfonamide functional groups enhance bioavailability and metabolic stability in drug formulations. Commonly employed in late-stage synthesis due to its chiral centers and functional group compatibility with peptide-like frameworks.

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