5-Chloro-7-iodo-8-methoxyquinoline

95%

Reagent Code: #128256
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CAS Number 91240-91-4

science Other reagents with same CAS 91240-91-4

blur_circular Chemical Specifications

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Weight 319.53 g/mol
Formula C₁₀H₇ClINO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial, antibacterial, and antifungal agents. Its quinoline structure with chloro, iodo, and methoxy groups enables selective modifications and effective interaction with microbial targets, making it valuable in medicinal chemistry for optimizing drug potency and bioavailability. Also employed in research settings to develop novel quinoline-based therapeutics targeting infectious diseases. Additionally, utilized as a reagent in organic synthesis, especially in cross-coupling reactions to replace the iodine atom with other functional groups.

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inventory 1g
10-20 days ฿27,000.00

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5-Chloro-7-iodo-8-methoxyquinoline
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial, antibacterial, and antifungal agents. Its quinoline structure with chloro, iodo, and methoxy groups enables selective modifications and effective interaction with microbial targets, making it valuable in medicinal chemistry for optimizing drug potency and bioavailability. Also employed in research settings to develop novel quinoline-based therapeutics targeting infectious diseases. Addit
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial, antibacterial, and antifungal agents. Its quinoline structure with chloro, iodo, and methoxy groups enables selective modifications and effective interaction with microbial targets, making it valuable in medicinal chemistry for optimizing drug potency and bioavailability. Also employed in research settings to develop novel quinoline-based therapeutics targeting infectious diseases. Additionally, utilized as a reagent in organic synthesis, especially in cross-coupling reactions to replace the iodine atom with other functional groups.
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