6-Bromo-4-chloro-2-(methylsulfanyl)quinazoline

≥95%

Reagent Code: #150643
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CAS Number 1003043-76-2

science Other reagents with same CAS 1003043-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.58 g/mol
Formula C₉H₆BrClN₂S
badge Registry Numbers
MDL Number MFCD11044642
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an 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 due to its halogenated quinazoline core, which allows for selective cross-coupling reactions. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its structural features make it valuable in structure-activity relationship (SAR) studies for drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,860.00

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6-Bromo-4-chloro-2-(methylsulfanyl)quinazoline
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Used as an 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 due to its halogenated quinazoline core, which allows for selective cross-coupling reactions. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its structural features make it valuable

Used as an 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 due to its halogenated quinazoline core, which allows for selective cross-coupling reactions. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinases and other enzyme families involved in signal transduction pathways. Its structural features make it valuable in structure-activity relationship (SAR) studies for drug discovery.

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