3-(2-Chloroethyl)quinazoline-2,4(1H,3H)-dione

97%

Reagent Code: #117384
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CAS Number 5081-87-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.64 g/mol
Formula C₁₀H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD00044732
thermostat Physical Properties
Melting Point 194-197°C
inventory_2 Storage & Handling
Density 1.358g/cm3
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its quinazoline-dione core structure is particularly valuable in the development of potential therapeutic agents, especially those targeting enzymes or receptors involved in disease pathways. Researchers often modify this compound to create derivatives that exhibit anticancer, antimicrobial, or anti-inflammatory properties. Additionally, its chloroethyl group provides a reactive site for further chemical transformations, enabling the attachment of diverse functional groups to enhance pharmacological activity or optimize drug-like properties. This makes it a versatile building block in drug discovery and development processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿801.00
inventory 1g
10-20 days ฿1,989.00
inventory 5g
10-20 days ฿6,129.00
3-(2-Chloroethyl)quinazoline-2,4(1H,3H)-dione
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its quinazoline-dione core structure is particularly valuable in the development of potential therapeutic agents, especially those targeting enzymes or receptors involved in disease pathways. Researchers often modify this compound to create derivatives that exhibit anticancer, antimicrobial, or anti-inflammatory properties. Additionally, its chloroethyl group provides a reactive site for further chemical transformations, enabling the attachment of diverse functional groups to enhance pharmacological activity or optimize drug-like properties. This makes it a versatile building block in drug discovery and development processes.
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