7-(Benzyloxy)-N-(4-bromo-2-fluorophenyl)-6-methoxyquinazolin-4-amine

≥95%

Reagent Code: #120805
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CAS Number 768350-54-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.29 g/mol
Formula C₂₂H₁₇BrFN₃O₂
badge Registry Numbers
MDL Number MFCD19440903
thermostat Physical Properties
Boiling Point 541.094°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of targeted therapeutic agents, particularly in the development of kinase inhibitors. Kinase inhibitors are crucial in treating various types of cancers, as they block specific enzymes involved in the growth and proliferation of cancer cells. The structural features of this compound, including the quinazoline core and substituted aromatic rings, make it a valuable scaffold for designing molecules that can selectively inhibit tyrosine kinases or other related enzymes. Researchers often modify and optimize this compound to enhance its binding affinity, selectivity, and pharmacokinetic properties, aiming to create effective and safe drugs for oncology applications. Additionally, its bromo and fluoro substituents provide reactive sites for further chemical modifications, enabling the exploration of diverse derivatives with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,904.00
inventory 250mg
10-20 days ฿9,846.00
inventory 1g
10-20 days ฿32,805.00
7-(Benzyloxy)-N-(4-bromo-2-fluorophenyl)-6-methoxyquinazolin-4-amine
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of targeted therapeutic agents, particularly in the development of kinase inhibitors. Kinase inhibitors are crucial in treating various types of cancers, as they block specific enzymes involved in the growth and proliferation of cancer cells. The structural features of this compound, including the quinazoline core and substituted aromatic rings, make it a valuable scaffold for designing molecules that can selectively inhibit tyrosine kinases or other related enzymes. Researchers often modify and optimize this compound to enhance its binding affinity, selectivity, and pharmacokinetic properties, aiming to create effective and safe drugs for oncology applications. Additionally, its bromo and fluoro substituents provide reactive sites for further chemical modifications, enabling the exploration of diverse derivatives with potential biological activity.
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