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

95%

Reagent Code: #51609
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CAS Number 1693955-94-0

science Other reagents with same CAS 1693955-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.1060 g/mol
Formula C₁₁H₉BrN₂O
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development due to its potential as a key intermediate in the synthesis of biologically active molecules. Its quinazolinone core structure is particularly valuable in the design of compounds targeting enzyme inhibition, making it a candidate for drug discovery in areas such as oncology and inflammation. Researchers explore its modifications to develop novel therapeutic agents, particularly in the development of kinase inhibitors, which are crucial in cancer treatment. Additionally, its bromo and cyclopropyl substituents offer opportunities for further chemical transformations, enabling the creation of diverse derivatives for biological evaluation. Its application extends to medicinal chemistry, where it serves as a building block for the development of new drugs with potential anti-tumor, anti-inflammatory, or anti-microbial properties.

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Test Parameter Specification
Appearance Light Brown Powder
Purity (%) 94.5-100%
MS Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,681.00

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7-Bromo-2-cyclopropylquinazolin-4(3H)-one
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This compound is primarily utilized in pharmaceutical research and development due to its potential as a key intermediate in the synthesis of biologically active molecules. Its quinazolinone core structure is particularly valuable in the design of compounds targeting enzyme inhibition, making it a candidate for drug discovery in areas such as oncology and inflammation. Researchers explore its modifications to develop novel therapeutic agents, particularly in the development of kinase inhibitors, which are crucial in cancer treatment. Additionally, its bromo and cyclopropyl substituents offer opportunities for further chemical transformations, enabling the creation of diverse derivatives for biological evaluation. Its application extends to medicinal chemistry, where it serves as a building block for the development of new drugs with potential anti-tumor, anti-inflammatory, or anti-microbial properties.
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