3-(2-Chlorophenyl)-6-Fluoro-2-Methyl-4(3H)-Quinazolinone

95%

Reagent Code: #82449
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CAS Number 49579-12-6

science Other reagents with same CAS 49579-12-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.70 g/mol
Formula C₁₅H₁₀ClFN₂O
badge Registry Numbers
MDL Number MFCD01686277
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural framework is particularly valuable in the development of quinazoline derivatives, which are known for their diverse biological activities. Specifically, it has been explored for its potential role in creating compounds with anti-inflammatory, anticancer, and antimicrobial properties. Researchers have also investigated its use in designing molecules that can inhibit specific enzymes or receptors, making it a promising candidate for drug discovery programs targeting diseases such as cancer and inflammatory disorders. Additionally, its fluorinated and chlorinated aromatic components contribute to its stability and bioavailability, enhancing its efficacy in therapeutic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,210.00
inventory 250mg
10-20 days ฿25,740.00
inventory 1g
10-20 days ฿52,200.00

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3-(2-Chlorophenyl)-6-Fluoro-2-Methyl-4(3H)-Quinazolinone
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural framework is particularly valuable in the development of quinazoline derivatives, which are known for their diverse biological activities. Specifically, it has been explored for its potential role in creating compounds with anti-inflammatory, anticancer, and antimicrobial properties. Researchers have also investigated its use in designing molecule

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural framework is particularly valuable in the development of quinazoline derivatives, which are known for their diverse biological activities. Specifically, it has been explored for its potential role in creating compounds with anti-inflammatory, anticancer, and antimicrobial properties. Researchers have also investigated its use in designing molecules that can inhibit specific enzymes or receptors, making it a promising candidate for drug discovery programs targeting diseases such as cancer and inflammatory disorders. Additionally, its fluorinated and chlorinated aromatic components contribute to its stability and bioavailability, enhancing its efficacy in therapeutic applications.

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