2,4,8-Trichloro-6-fluoroquinazoline

97%

Reagent Code: #242260
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CAS Number 1702815-70-0

science Other reagents with same CAS 1702815-70-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.47 g/mol
Formula C₈H₂Cl₃FN₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic core, which enhances binding to biological targets. The compound’s reactivity profile supports functionalization at multiple sites, enabling fine-tuning of molecular properties in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,480.00
inventory 250mg
10-20 days ฿15,470.00

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2,4,8-Trichloro-6-fluoroquinazoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic core, which enhances binding to biological targets. The compound’s

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the development of kinase inhibitors and other bioactive molecules. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. It is also employed in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic core, which enhances binding to biological targets. The compound’s reactivity profile supports functionalization at multiple sites, enabling fine-tuning of molecular properties in drug discovery programs.

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