(1S,4R)-(4-Aminocyclopent-2-enyl)methanol hydrochloride

98%

Reagent Code: #234750
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CAS Number 168960-19-8

science Other reagents with same CAS 168960-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.61 g/mol
Formula C₆H₁₁NO·HCl
badge Registry Numbers
MDL Number MFCD01632106
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in the synthesis of antiviral and antiretroviral drugs, particularly as a key intermediate in the production of nucleoside analogs. Its structural features make it valuable in medicinal chemistry for developing compounds that interfere with viral replication. Commonly employed in research settings to design new therapeutic agents targeting RNA and DNA viruses. Also utilized in the preparation of chiral building blocks for pharmaceuticals, contributing to the stereochemical control needed in drug development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿1,510.00
inventory 100g
10-20 days ฿5,900.00
inventory 500g
10-20 days ฿28,900.00
(1S,4R)-(4-Aminocyclopent-2-enyl)methanol hydrochloride
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Used in the synthesis of antiviral and antiretroviral drugs, particularly as a key intermediate in the production of nucleoside analogs. Its structural features make it valuable in medicinal chemistry for developing compounds that interfere with viral replication. Commonly employed in research settings to design new therapeutic agents targeting RNA and DNA viruses. Also utilized in the preparation of chiral building blocks for pharmaceuticals, contributing to the stereochemical control needed in drug develo
Used in the synthesis of antiviral and antiretroviral drugs, particularly as a key intermediate in the production of nucleoside analogs. Its structural features make it valuable in medicinal chemistry for developing compounds that interfere with viral replication. Commonly employed in research settings to design new therapeutic agents targeting RNA and DNA viruses. Also utilized in the preparation of chiral building blocks for pharmaceuticals, contributing to the stereochemical control needed in drug development.
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