N2-(3-Chloro-4-methylphenyl)quinazoline-2,4-diamine

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Reagent Code: #52951
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CAS Number 1001625-82-6

science Other reagents with same CAS 1001625-82-6

blur_circular Chemical Specifications

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Weight 284.7435 g/mol
Formula C₁₅H₁₃ClN₄
badge Registry Numbers
MDL Number MFCD05840188
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors involved in disease pathways. Its quinazoline core structure is often explored for developing inhibitors of tyrosine kinases, which play a critical role in cancer cell proliferation and survival. Researchers also investigate its derivatives for potential applications in treating inflammatory diseases and other conditions where modulation of cellular signaling pathways is beneficial. Additionally, its structural features make it a valuable candidate for further chemical modifications to enhance drug-like properties, such as bioavailability and target specificity.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿12,960.00

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N2-(3-Chloro-4-methylphenyl)quinazoline-2,4-diamine
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors involved in disease pathways. Its quinazoline core structure is often explored for developing inhibitors of tyrosine kinases, which play a critical role in cancer cell proliferation and survival. Researchers also investigate its derivatives for potential applications in treating inflammatory diseases and other conditions where modulation of cellular signaling pathways is beneficial. Additionally, its structural features make it a valuable candidate for further chemical modifications to enhance drug-like properties, such as bioavailability and target specificity.
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