methyl (1R,4S)-4-aminocyclopent-2-ene-1-carboxylate hydrochloride

97%

Reagent Code: #228724
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CAS Number 426226-35-9

science Other reagents with same CAS 426226-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.63 g/mol
Formula C₇H₁₂ClNO₂
badge Registry Numbers
MDL Number MFCD18207147
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C therapeutics. Its enantiomerically pure structure enables selective reactions in multi-step organic syntheses, improving yield and purity of the final active pharmaceutical ingredient. Commonly employed in medicinal chemistry for constructing cyclopentane-based nucleoside analogs that mimic natural ribose sugars, enhancing metabolic stability and target binding. Also utilized in the development of protease inhibitors due to its rigid cyclic framework and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿1,650.00
inventory 1g
10-20 days ฿2,640.00
methyl (1R,4S)-4-aminocyclopent-2-ene-1-carboxylate hydrochloride
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Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C therapeutics. Its enantiomerically pure structure enables selective reactions in multi-step organic syntheses, improving yield and purity of the final active pharmaceutical ingredient. Commonly employed in medicinal chemistry for constructing cyclopentane-based nucleoside analogs that mimic natural ribose sugars, enhancing metabolic stability and target binding. Also utilized in the develo

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of hepatitis C therapeutics. Its enantiomerically pure structure enables selective reactions in multi-step organic syntheses, improving yield and purity of the final active pharmaceutical ingredient. Commonly employed in medicinal chemistry for constructing cyclopentane-based nucleoside analogs that mimic natural ribose sugars, enhancing metabolic stability and target binding. Also utilized in the development of protease inhibitors due to its rigid cyclic framework and functional group compatibility.

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