8-Bromoquinoline-5-sulfonyl chloride

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Reagent Code: #151485
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CAS Number 930396-14-8

science Other reagents with same CAS 930396-14-8

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scatter_plot Molecular Information
Weight 306.56 g/mol
Formula C₉H₅BrClNO₂S
badge Registry Numbers
MDL Number MFCD09742562
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of sulfonamide-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo and sulfonyl chloride functional groups allow selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of fluorescent probes for bioimaging, leveraging the quinoline core’s inherent photophysical properties.

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inventory 250mg
10-20 days ฿20,280.00

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8-Bromoquinoline-5-sulfonyl chloride
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Used as a key intermediate in the synthesis of sulfonamide-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo and sulfonyl chloride functional groups allow selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation

Used as a key intermediate in the synthesis of sulfonamide-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its bromo and sulfonyl chloride functional groups allow selective derivatization, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of fluorescent probes for bioimaging, leveraging the quinoline core’s inherent photophysical properties.

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