3-Benzyl-7-bromo-2-methoxyquinoline

98%

Reagent Code: #124220
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CAS Number 918648-51-8

science Other reagents with same CAS 918648-51-8

blur_circular Chemical Specifications

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Weight 328.2 g/mol
Formula C₁₇H₁₄BrNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with functional groups like bromo and methoxy, makes it a versatile building block for developing compounds with potential pharmacological properties. Researchers often employ it in the design and synthesis of drug candidates targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿33,345.00
inventory 100mg
10-20 days ฿10,035.00
inventory 250mg
10-20 days ฿16,704.00

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3-Benzyl-7-bromo-2-methoxyquinoline
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with functional groups like bromo and methoxy, makes it a versatile building block for developing compounds with potential pharmacological properties. Researchers often employ it in the design and synthesis of drug candidates targeting specific enzymes or receptors, particularly in the development of anti-inflamm

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a quinoline core with functional groups like bromo and methoxy, makes it a versatile building block for developing compounds with potential pharmacological properties. Researchers often employ it in the design and synthesis of drug candidates targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, antimicrobial, or anticancer agents. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery efforts.

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