Ethyl 5-nitropyrimidine-2-carboxylate

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Reagent Code: #183656
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CAS Number 1894988-20-5

science Other reagents with same CAS 1894988-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.15 g/mol
Formula C₇H₇N₃O₄
badge Registry Numbers
MDL Number MFCD30475679
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. The nitro group at position 5 and the ethyl carboxylate at position 2 enable diverse functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based drug candidates. Commonly employed in reactions involving nucleophilic substitution or cyclization to form fused heterocyclic systems. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or herbicidal activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,600.00
inventory 250mg
10-20 days ฿9,890.00
inventory 1g
10-20 days ฿24,700.00

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Ethyl 5-nitropyrimidine-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. The nitro group at position 5 and the ethyl carboxylate at position 2 enable diverse functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based drug candidates. Commonly employed in reactions involving nucleophilic substitution or cyclization to form fused heterocyclic systems. Also utilized in agrochemical research for de
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. The nitro group at position 5 and the ethyl carboxylate at position 2 enable diverse functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based drug candidates. Commonly employed in reactions involving nucleophilic substitution or cyclization to form fused heterocyclic systems. Also utilized in agrochemical research for designing bioactive molecules with pesticidal or herbicidal activity.
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