4-chloro-5-iodopyrimidine

≥97%

Reagent Code: #159395
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CAS Number 63558-65-6

science Other reagents with same CAS 63558-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.43 g/mol
Formula C₄H₂ClIN₂
badge Registry Numbers
MDL Number MFCD08276157
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas environment

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in creating active ingredients in drug discovery. Commonly employed in cross-coupling reactions to build complex pyrimidine-based molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its halogen atoms enable efficient derivatization through substitution reactions, supporting rapid compound optimization in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,380.00
5g
10-20 days ฿5,910.00
25g
10-20 days ฿19,960.00
100g
10-20 days ฿69,860.00
4-chloro-5-iodopyrimidine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in creating active ingredients in drug discovery. Commonly employed in cross-coupling reactions to build complex pyrimidine-based molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its halogen atoms enable efficient derivatization through substitution reactions

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in creating active ingredients in drug discovery. Commonly employed in cross-coupling reactions to build complex pyrimidine-based molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its halogen atoms enable efficient derivatization through substitution reactions, supporting rapid compound optimization in medicinal chemistry.

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