7-Bromo-8-fluoro-6-iodoquinazoline-2,4(1H,3H)-dione

98%

Reagent Code: #141641
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CAS Number 2241721-74-2

science Other reagents with same CAS 2241721-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.9285 g/mol
Formula C₈H₃BrFIN₂O₂
inventory_2 Storage & Handling
Density 2.350±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of quinazoline-based pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its halogen substitution pattern allows for selective cross-coupling reactions, enabling the introduction of functional groups to optimize biological activity. Commonly employed in medicinal chemistry research for generating novel analogs with potential antitumor and anti-inflammatory properties. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to its reactive halogens and stable heterocyclic core.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,200.00
inventory 500mg
10-20 days ฿4,630.00
inventory 1g
10-20 days ฿6,400.00
inventory 5g
10-20 days ฿19,200.00
inventory 25g
10-20 days ฿72,000.00

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7-Bromo-8-fluoro-6-iodoquinazoline-2,4(1H,3H)-dione
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Used as a key intermediate in the synthesis of quinazoline-based pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its halogen substitution pattern allows for selective cross-coupling reactions, enabling the introduction of functional groups to optimize biological activity. Commonly employed in medicinal chemistry research for generating novel analogs with potential antitumor and anti-inflammatory properties. Also utilized in the preparation of fluorescent

Used as a key intermediate in the synthesis of quinazoline-based pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its halogen substitution pattern allows for selective cross-coupling reactions, enabling the introduction of functional groups to optimize biological activity. Commonly employed in medicinal chemistry research for generating novel analogs with potential antitumor and anti-inflammatory properties. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to its reactive halogens and stable heterocyclic core.

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