6-bromo-2-[4-(carboxymethoxy)phenyl]quinoline-4-carboxylic acid

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Reagent Code: #141768
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CAS Number 892218-43-8

science Other reagents with same CAS 892218-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.1956 g/mol
Formula C₁₈H₁₂BrNO₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of anticancer and antimicrobial agents. Derivatives exhibit properties to inhibit certain enzymes, such as tyrosine kinases, which are involved in cancer cell proliferation. Its functional groups enable conjugation in targeted drug delivery systems, enhancing selectivity and efficacy by allowing binding to specific cell surface receptors. Also employed in research for designing fluorescent probes due to the quinoline scaffold’s photophysical properties, useful in cellular imaging and biochemical assays.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,400.00
inventory 100mg
10-20 days ฿40,000.00

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6-bromo-2-[4-(carboxymethoxy)phenyl]quinoline-4-carboxylic acid
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of anticancer and antimicrobial agents. Derivatives exhibit properties to inhibit certain enzymes, such as tyrosine kinases, which are involved in cancer cell proliferation. Its functional groups enable conjugation in targeted drug delivery systems, enhancing selectivity and efficacy by allowing binding to specific cell surface receptors. Also employed in research for designing fluorescent prob

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of anticancer and antimicrobial agents. Derivatives exhibit properties to inhibit certain enzymes, such as tyrosine kinases, which are involved in cancer cell proliferation. Its functional groups enable conjugation in targeted drug delivery systems, enhancing selectivity and efficacy by allowing binding to specific cell surface receptors. Also employed in research for designing fluorescent probes due to the quinoline scaffold’s photophysical properties, useful in cellular imaging and biochemical assays.

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