2,4-Dichloro-6-methoxyquinoline

98%

Reagent Code: #171460
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CAS Number 70049-46-6

science Other reagents with same CAS 70049-46-6

blur_circular Chemical Specifications

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Weight 228.08 g/mol
Formula C₁₀H₇Cl₂NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. It serves as a building block in the preparation of quinoline-based compounds that exhibit biological activity against Plasmodium species. Also employed in research for the design of kinase inhibitors and other bioactive molecules due to its ability to participate in selective substitution reactions. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates with improved potency and metabolic stability.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,410.00
inventory 250mg
10-20 days ฿4,280.00
inventory 1g
10-20 days ฿10,630.00
inventory 5g
10-20 days ฿35,230.00

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2,4-Dichloro-6-methoxyquinoline
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. It serves as a building block in the preparation of quinoline-based compounds that exhibit biological activity against Plasmodium species. Also employed in research for the design of kinase inhibitors and other bioactive molecules due to its ability to participate in selective substitution reactions. Its structural features make it valuable in medicinal chemistry for optimizing drug candida

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial drugs. It serves as a building block in the preparation of quinoline-based compounds that exhibit biological activity against Plasmodium species. Also employed in research for the design of kinase inhibitors and other bioactive molecules due to its ability to participate in selective substitution reactions. Its structural features make it valuable in medicinal chemistry for optimizing drug candidates with improved potency and metabolic stability.

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