3-Bromo-7-(methylsulfonyl)quinoline

97%

Reagent Code: #151462
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CAS Number 1956331-49-9

science Other reagents with same CAS 1956331-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.15 g/mol
Formula C₁₀H₈BrNO₂S
badge Registry Numbers
MDL Number MFCD29059318
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research for designing fluorescent probes due to its quinoline backbone, which supports photostability and signal detection in biological imaging. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting inflammatory and oncological pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,380.00
inventory 250mg
10-20 days ฿38,980.00

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3-Bromo-7-(methylsulfonyl)quinoline
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research for designing fluorescent probes due to its quinoline backbone, which supports photostability and signal detection in biological imaging. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research for designing fluorescent probes due to its quinoline backbone, which supports photostability and signal detection in biological imaging. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting inflammatory and oncological pathways.

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