Ethyl 4,7-dichloro-8-methylquinoline-3-carboxylate

95%

Reagent Code: #184598
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CAS Number 58666-08-3

science Other reagents with same CAS 58666-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.14 g/mol
Formula C₁₃H₁₁Cl₂NO₂
badge Registry Numbers
MDL Number MFCD00173378
thermostat Physical Properties
Boiling Point 376.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.344±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the quinoline core, which is known for its pharmacological activity. It is also employed in research settings for the preparation of novel heterocyclic compounds with potential antimicrobial and anticancer properties. The ester and chloro functional groups allow for further chemical modifications, making it valuable in medicinal chemistry and drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,140.00
inventory 250mg
10-20 days ฿7,950.00
inventory 1g
10-20 days ฿17,320.00

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Ethyl 4,7-dichloro-8-methylquinoline-3-carboxylate
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the quinoline core, which is known for its pharmacological activity. It is also employed in research settings for the preparation of novel heterocyclic compounds with potential antimicrobial and anticancer properties. The ester and chloro functional groups allow for further chemical modifications, making it

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the quinoline core, which is known for its pharmacological activity. It is also employed in research settings for the preparation of novel heterocyclic compounds with potential antimicrobial and anticancer properties. The ester and chloro functional groups allow for further chemical modifications, making it valuable in medicinal chemistry and drug design.

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