6-Bromo-2-(5-methylfuran-2-yl)quinoline-4-carboxylic acid

95%

Reagent Code: #141363
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CAS Number 350998-12-8

science Other reagents with same CAS 350998-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.16 g/mol
Formula C₁₅H₁₀BrNO₃
badge Registry Numbers
MDL Number MFCD01922680
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency in targeted therapies. Also employed in research settings to design novel heterocyclic compounds with potential antimicrobial and anti-inflammatory activities. The bromine moiety allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug-like molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,930.00
inventory 250mg
10-20 days ฿11,770.00
inventory 1g
10-20 days ฿31,770.00

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6-Bromo-2-(5-methylfuran-2-yl)quinoline-4-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency in targeted therapies. Also employed in research settings to design novel heterocyclic compounds with potential antimicrobial and anti-inflammatory activities. The bromine moiety allows for further functionalization via cross-coupling reactions, making it valuable i

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency in targeted therapies. Also employed in research settings to design novel heterocyclic compounds with potential antimicrobial and anti-inflammatory activities. The bromine moiety allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug-like molecules.

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