6-Iodoquinazoline-2,4(1H,3H)-dione

≥95%

Reagent Code: #200038
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CAS Number 16353-27-8

science Other reagents with same CAS 16353-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.04 g/mol
Formula C₈H₅IN₂O₂
badge Registry Numbers
MDL Number MFCD09029814
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active quinazoline derivatives, particularly in pharmaceutical research targeting kinase inhibitors. Its iodo functional group allows for facile cross-coupling reactions, enabling the introduction of various substituents to modify potency and selectivity in drug candidates. Commonly employed in the development of anticancer, antiviral, and anti-inflammatory agents due to the quinazoline core’s affinity for enzyme inhibition. Also utilized in labeled compound synthesis for metabolic studies and imaging probes owing to the presence of iodine.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,260.00
6-Iodoquinazoline-2,4(1H,3H)-dione
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Used as a key intermediate in the synthesis of biologically active quinazoline derivatives, particularly in pharmaceutical research targeting kinase inhibitors. Its iodo functional group allows for facile cross-coupling reactions, enabling the introduction of various substituents to modify potency and selectivity in drug candidates. Commonly employed in the development of anticancer, antiviral, and anti-inflammatory agents due to the quinazoline core’s affinity for enzyme inhibition. Also utilized in lab

Used as a key intermediate in the synthesis of biologically active quinazoline derivatives, particularly in pharmaceutical research targeting kinase inhibitors. Its iodo functional group allows for facile cross-coupling reactions, enabling the introduction of various substituents to modify potency and selectivity in drug candidates. Commonly employed in the development of anticancer, antiviral, and anti-inflammatory agents due to the quinazoline core’s affinity for enzyme inhibition. Also utilized in labeled compound synthesis for metabolic studies and imaging probes owing to the presence of iodine.

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