1-(Prop-2-yn-1-yl)pyrimidine-2, 4(1H, 3H)-dione

97%

Reagent Code: #227307
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CAS Number 168413-01-2

science Other reagents with same CAS 168413-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₇H₆N₂O₂
badge Registry Numbers
MDL Number MFCD14638450
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of antiviral and anticancer agents. Its structure supports the development of nucleoside analogs that interfere with viral replication or tumor cell proliferation. Commonly employed in medicinal chemistry for modifying pyrimidine-based compounds to enhance biological activity and selectivity. The alkyne functionality enables efficient incorporation into click chemistry reactions for creating hybrid compounds or molecular labeling in biomolecular research. Also utilized in research for designing new small-molecule therapeutics targeting RNA viruses and certain enzyme pathways involved in DNA synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,500.00
250mg
10-20 days ฿11,050.00
1g
10-20 days ฿32,300.00
1-(Prop-2-yn-1-yl)pyrimidine-2, 4(1H, 3H)-dione
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Used as a key intermediate in the synthesis of antiviral and anticancer agents. Its structure supports the development of nucleoside analogs that interfere with viral replication or tumor cell proliferation. Commonly employed in medicinal chemistry for modifying pyrimidine-based compounds to enhance biological activity and selectivity. The alkyne functionality enables efficient incorporation into click chemistry reactions for creating hybrid compounds or molecular labeling in biomolecular research. Also

Used as a key intermediate in the synthesis of antiviral and anticancer agents. Its structure supports the development of nucleoside analogs that interfere with viral replication or tumor cell proliferation. Commonly employed in medicinal chemistry for modifying pyrimidine-based compounds to enhance biological activity and selectivity. The alkyne functionality enables efficient incorporation into click chemistry reactions for creating hybrid compounds or molecular labeling in biomolecular research. Also utilized in research for designing new small-molecule therapeutics targeting RNA viruses and certain enzyme pathways involved in DNA synthesis.

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