4-Chloro-7-(trifluoromethoxy)quinazoline

≥95%

Reagent Code: #86140
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CAS Number 1160994-87-5

science Other reagents with same CAS 1160994-87-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.59 g/mol
Formula C₉H₄ClF₃N₂O
badge Registry Numbers
MDL Number MFCD12400772
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

4-Chloro-7-(trifluoromethoxy)quinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinazoline core structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeting specific enzymes involved in signal transduction pathways. This compound is often employed in the design and production of potential therapeutic agents for treating diseases such as cancer, where kinase activity is dysregulated. Additionally, its unique substitution pattern, including the chloro and trifluoromethoxy groups, enhances its reactivity and selectivity in chemical reactions, making it a versatile building block for further modifications. Researchers also explore its applications in creating novel pharmaceuticals with improved efficacy and reduced side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,841.00
inventory 100mg
10-20 days ฿3,312.00
inventory 1g
10-20 days ฿20,475.00

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4-Chloro-7-(trifluoromethoxy)quinazoline
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4-Chloro-7-(trifluoromethoxy)quinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinazoline core structure is particularly valuable in the development of kinase inhibitors, which are crucial in targeting specific enzymes involved in signal transduction pathways. This compound is often employed in the design and production of potential therapeutic agents for treating diseases such as cancer, where kinase activity is dysregulated. Additionally, its unique substitution pattern, including the chloro and trifluoromethoxy groups, enhances its reactivity and selectivity in chemical reactions, making it a versatile building block for further modifications. Researchers also explore its applications in creating novel pharmaceuticals with improved efficacy and reduced side effects.
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