5-Iodo-6-methyl-2-(methylthio)-1H-pyrimidin-4-one

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Reagent Code: #200407
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CAS Number 76510-64-0

science Other reagents with same CAS 76510-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.1 g/mol
Formula C₆H₇IN₂OS
badge Registry Numbers
MDL Number MFCD01150903
thermostat Physical Properties
Melting Point 209-212 °C (decomposition)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure allows for selective modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in nucleoside analog synthesis, where the iodo group facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in research settings to study enzyme inhibition, especially in thymidylate synthase and related metabolic pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,230.00
5-Iodo-6-methyl-2-(methylthio)-1H-pyrimidin-4-one
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure allows for selective modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in nucleoside analog synthesis, where the iodo group facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in research settings to study enzyme inhibition, especially in thymidylate synthase and r

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and anticancer agents. Its structure allows for selective modifications, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in nucleoside analog synthesis, where the iodo group facilitates coupling reactions such as Suzuki or Stille cross-couplings. Also utilized in research settings to study enzyme inhibition, especially in thymidylate synthase and related metabolic pathways.

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