4-Chloro-5-(trifluoromethyl)quinazoline

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Reagent Code: #119144
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CAS Number 16499-63-1

science Other reagents with same CAS 16499-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.59 g/mol
Formula C₉H₄ClF₃N₂
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its quinazoline core structure is particularly valuable in designing inhibitors for enzymes like tyrosine kinases, which are targeted in cancer therapies. Additionally, it finds application in the development of antimicrobial and antiviral agents due to its ability to interact with specific protein structures. The trifluoromethyl group enhances its metabolic stability and binding affinity, making it a crucial component in the creation of potent and selective drugs. Furthermore, it is being studied in agricultural chemistry for the development of highly effective and safer pesticides.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,155.00
inventory 250mg
10-20 days ฿9,963.00
inventory 1g
10-20 days ฿17,874.00

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4-Chloro-5-(trifluoromethyl)quinazoline
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its quinazoline core structure is particularly valuable in designing inhibitors for enzymes like tyrosine kinases, which are targeted in cancer therapies. Additionally, it finds application in the development of antimicrobial and antiviral agents due to its ability to interact with specific protein structures. The trifluoromethyl group enhances i

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its quinazoline core structure is particularly valuable in designing inhibitors for enzymes like tyrosine kinases, which are targeted in cancer therapies. Additionally, it finds application in the development of antimicrobial and antiviral agents due to its ability to interact with specific protein structures. The trifluoromethyl group enhances its metabolic stability and binding affinity, making it a crucial component in the creation of potent and selective drugs. Furthermore, it is being studied in agricultural chemistry for the development of highly effective and safer pesticides.

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