5-Iodopyrimidin-2(1H)-one

95%

Reagent Code: #199796
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CAS Number 79387-69-2

science Other reagents with same CAS 79387-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.98 g/mol
Formula C₄H₃IN₂O
inventory_2 Storage & Handling
Storage 2-8°C

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 selective modifications, making it valuable in medicinal chemistry for creating pyrimidine-based drug candidates. Commonly employed in nucleoside analog synthesis where the iodine moiety facilitates coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aromatic or heteroaromatic groups. Also utilized in research settings for labeling and tracer studies due to the presence of iodine, which can be easily detected or radio-labeled.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿170.50
250mg
10-20 days ฿176.00
1g
10-20 days ฿429.00
5g
10-20 days ฿1,914.00
5-Iodopyrimidin-2(1H)-one
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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 selective modifications, making it valuable in medicinal chemistry for creating pyrimidine-based drug candidates. Commonly employed in nucleoside analog synthesis where the iodine moiety facilitates coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aromatic or heteroaromatic groups. Also utilized in research settings f

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating pyrimidine-based drug candidates. Commonly employed in nucleoside analog synthesis where the iodine moiety facilitates coupling reactions such as Suzuki or Heck reactions, enabling the introduction of aromatic or heteroaromatic groups. Also utilized in research settings for labeling and tracer studies due to the presence of iodine, which can be easily detected or radio-labeled.

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