6-Iodo-4-(3-Methoxyphenylamino)-8-Methylquinoline-3-Carboxamide

95%

Reagent Code: #200954
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CAS Number 801315-47-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 433.24 g/mol
Formula C₁₈H₁₆IN₃O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in the development of targeted therapies for solid tumors due to its ability to modulate signaling pathways. Also employed in structure-activity relationship (SAR) studies to optimize antitumor activity and selectivity in quinoline-based drug candidates.

Additionally, it serves as a starting material or intermediate in the laboratory synthesis of other bioactive compounds, owing to its iodine group which enables further reactions, such as cross-coupling, to generate new derivatives with therapeutic potential.

Currently, it is not used in commercial or direct medical applications, remaining in the stage of laboratory studies and testing.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,680.00
6-Iodo-4-(3-Methoxyphenylamino)-8-Methylquinoline-3-Carboxamide
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in the development of targeted therapies for solid tumors due to its ability to modulate signaling pathways. Also employed in structure-activity relationship (SAR) studies to optimize antitumor activity and selectivity in quinoline-based drug candidates.

Additionally, it serves as a starting material or intermedia

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting tyrosine kinases involved in cancer cell proliferation. Shows potential in the development of targeted therapies for solid tumors due to its ability to modulate signaling pathways. Also employed in structure-activity relationship (SAR) studies to optimize antitumor activity and selectivity in quinoline-based drug candidates.

Additionally, it serves as a starting material or intermediate in the laboratory synthesis of other bioactive compounds, owing to its iodine group which enables further reactions, such as cross-coupling, to generate new derivatives with therapeutic potential.

Currently, it is not used in commercial or direct medical applications, remaining in the stage of laboratory studies and testing.

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