7-Bromo-2-methylquinazolin-4(3H)-one

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Reagent Code: #146214
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CAS Number 403850-89-5

science Other reagents with same CAS 403850-89-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.07 g/mol
Formula C₉H₇BrN₂O
badge Registry Numbers
MDL Number MFCD11043862
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for creating analogs with potential antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for selective modifications at multiple sites, enabling optimization of biological activity and pharmacokinetic properties in drug design. Commonly employed in research settings for structure-activity relationship (SAR) studies targeting oncology and central nervous system disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿3,220.00
inventory 25g
10-20 days ฿42,230.00
inventory 5g
10-20 days ฿11,160.00

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7-Bromo-2-methylquinazolin-4(3H)-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for creating analogs with potential antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for selective modifications at multiple sites, enabling optimization of biological activity and pharmacokinetic properties in drug design. Commonly employed in research settings for structure

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for creating analogs with potential antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for selective modifications at multiple sites, enabling optimization of biological activity and pharmacokinetic properties in drug design. Commonly employed in research settings for structure-activity relationship (SAR) studies targeting oncology and central nervous system disorders.

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