5-Bromo-N-(quinolin-8-yl)thiophene-2-sulfonamide

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Reagent Code: #49067
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CAS Number 620103-87-9

science Other reagents with same CAS 620103-87-9

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scatter_plot Molecular Information
Weight 369.2568 g/mol
Formula C₁₃H₉BrN₂O₂S₂
badge Registry Numbers
MDL Number MFCD06290688
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Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety and a thiophene sulfonamide group, makes it a valuable scaffold for developing inhibitors or modulators of protein-protein interactions. Researchers often explore its potential in designing compounds for anti-inflammatory, anticancer, or antimicrobial applications. Additionally, its unique chemical properties enable its use in studying biochemical pathways and validating drug targets in preclinical research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,078.00

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5-Bromo-N-(quinolin-8-yl)thiophene-2-sulfonamide
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This compound is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety and a thiophene sulfonamide group, makes it a valuable scaffold for developing inhibitors or modulators of protein-protein interactions. Researchers often explore its potential in designing compounds for anti-inflammatory, antican

This compound is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety and a thiophene sulfonamide group, makes it a valuable scaffold for developing inhibitors or modulators of protein-protein interactions. Researchers often explore its potential in designing compounds for anti-inflammatory, anticancer, or antimicrobial applications. Additionally, its unique chemical properties enable its use in studying biochemical pathways and validating drug targets in preclinical research.

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