Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate

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Reagent Code: #47161
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CAS Number 338954-49-7

science Other reagents with same CAS 338954-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.7200 g/mol
Formula C₁₄H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD00173354
thermostat Physical Properties
Boiling Point 363.3 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.222g/cm3
Storage room temperature

description Product Description

Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable scaffold for developing pharmaceuticals, particularly in the design of antimalarial and anticancer agents. Researchers leverage its chemical framework to create derivatives that can interact with specific biological targets, such as enzymes or receptors, to modulate disease pathways. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its role in drug discovery and development highlights its importance in advancing therapeutic innovations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,490.00

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Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate
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Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable scaffold for developing pharmaceuticals, particularly in the design of antimalarial and anticancer agents. Researchers leverage its chemical framework to create derivatives that can interact with specific biological targets, such as enzymes or receptors, to modulate dis

Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable scaffold for developing pharmaceuticals, particularly in the design of antimalarial and anticancer agents. Researchers leverage its chemical framework to create derivatives that can interact with specific biological targets, such as enzymes or receptors, to modulate disease pathways. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its role in drug discovery and development highlights its importance in advancing therapeutic innovations.

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