rel-(1R,4S)-4-Hydroxycyclopent-2-en-1-yl acetate

98%

Reagent Code: #232290
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CAS Number 60410-18-6

science Other reagents with same CAS 60410-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.15 g/mol
Formula C₇H₁₀O₃
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MDL Number MFCD00077637
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of cyclopentane-based nucleoside analogs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the preparation of prostaglandin analogs and other bioactive molecules where precise three-dimensional structure is critical for biological activity. Also utilized in research settings for asymmetric synthesis and catalysis studies due to its rigid cyclopentene backbone and functional group compatibility.

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inventory 100mg
10-20 days ฿10,950.00

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rel-(1R,4S)-4-Hydroxycyclopent-2-en-1-yl acetate
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Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of cyclopentane-based nucleoside analogs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the preparation of prostaglandin analogs and other bioactive molecules where precise three-dimensional structure is critical for biological activity. Also utilized in research settings for asymmetric synthesis

Used as a key chiral intermediate in the synthesis of antiviral drugs, particularly in the production of cyclopentane-based nucleoside analogs. Its stereochemistry allows for selective reactions in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the preparation of prostaglandin analogs and other bioactive molecules where precise three-dimensional structure is critical for biological activity. Also utilized in research settings for asymmetric synthesis and catalysis studies due to its rigid cyclopentene backbone and functional group compatibility.

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