Methyl 5-iodo-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate

95%

Reagent Code: #202894
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CAS Number 116393-71-6

science Other reagents with same CAS 116393-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.02 g/mol
Formula C₆H₅IN₂O₄
badge Registry Numbers
MDL Number MFCD12498716
inventory_2 Storage & Handling
Density 2.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based heterocycles. Commonly employed in nucleoside analog synthesis, where the iodine moiety facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in the preparation of kinase inhibitors and other biologically active molecules targeting cellular replication pathways. Its ester group enables further derivatization, enhancing solubility or bioavailability in drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,560.00
inventory 250mg
10-20 days ฿10,230.00
inventory 1g
10-20 days ฿24,240.00
inventory 5g
10-20 days ฿72,710.00
Methyl 5-iodo-2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based heterocycles. Commonly employed in nucleoside analog synthesis, where the iodine moiety facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in the preparation of kinase inhibitors and other biologically active m
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building pyrimidine-based heterocycles. Commonly employed in nucleoside analog synthesis, where the iodine moiety facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in the preparation of kinase inhibitors and other biologically active molecules targeting cellular replication pathways. Its ester group enables further derivatization, enhancing solubility or bioavailability in drug design.
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