3-Cyclopropyl-1-(2-fluoro-4-iodophenyl)-5-hydroxy-6,8-dimethylpyrido[2,3-d]pyrimidine-2,4,7(1H,3H,8H)-trione

97%

Reagent Code: #118097
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CAS Number 871700-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 483.23 g/mol
Formula C₁₈H₁₅FIN₃O₄
badge Registry Numbers
MDL Number MFCD18207185
thermostat Physical Properties
Boiling Point 518.2±60.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a pyrido[2,3-d]pyrimidine core, makes it a valuable scaffold for developing potential therapeutic agents. Researchers focus on its application in designing inhibitors targeting specific enzymes or receptors, particularly in the treatment of diseases such as cancer, inflammation, or microbial infections. The presence of functional groups like the cyclopropyl and fluoro-iodo-phenyl moieties enhances its binding affinity and selectivity, making it a promising candidate for drug discovery and optimization studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days £231.08
inventory 100mg
10-20 days £15.68
inventory 250mg
10-20 days £24.76
inventory 1g
10-20 days £63.34
3-Cyclopropyl-1-(2-fluoro-4-iodophenyl)-5-hydroxy-6,8-dimethylpyrido[2,3-d]pyrimidine-2,4,7(1H,3H,8H)-trione
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a pyrido[2,3-d]pyrimidine core, makes it a valuable scaffold for developing potential therapeutic agents. Researchers focus on its application in designing inhibitors targeting specific enzymes or receptors, particularly in the treatment of diseases such as cancer, inflammation, or microbial infections. The presence of functional groups like the cyclopropyl and fluoro-iodo-phenyl moieties enhances its binding affinity and selectivity, making it a promising candidate for drug discovery and optimization studies.
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