2-bromo-6-methylquinazolin-4(1H)-one

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Reagent Code: #82384
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CAS Number 1782469-69-5

science Other reagents with same CAS 1782469-69-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.07 g/mol
Formula C₉H₇BrN₂O
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural properties. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazolinone core is often explored for developing compounds with potential anticancer, antimicrobial, and anti-inflammatory properties. Researchers also investigate its derivatives for their ability to interact with specific protein targets, making it valuable in drug discovery and development processes. Additionally, its bromo and methyl substituents provide reactive sites for further chemical modifications, enabling the creation of diverse libraries of compounds for high-throughput screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,300.00
inventory 250mg
10-20 days ฿46,800.00

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2-bromo-6-methylquinazolin-4(1H)-one
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural properties. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazolinone core is often explored for developing compounds with potential anticancer, antimicrobial, and anti-inflammatory properties. Researchers also investigate its derivatives for their ability to interact with specific prote

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural properties. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazolinone core is often explored for developing compounds with potential anticancer, antimicrobial, and anti-inflammatory properties. Researchers also investigate its derivatives for their ability to interact with specific protein targets, making it valuable in drug discovery and development processes. Additionally, its bromo and methyl substituents provide reactive sites for further chemical modifications, enabling the creation of diverse libraries of compounds for high-throughput screening.

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