ethyl 4-hydroxy-6-methoxy-8-methylquinoline-3-carboxylate

95%

Reagent Code: #184739
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CAS Number 384820-98-8

science Other reagents with same CAS 384820-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.27 g/mol
Formula C₁₄H₁₅NO₄
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MDL Number MFCD28138077
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of reactive functional groups—hydroxy, methoxy, and ester—that allow for further chemical modifications. Commonly employed in medicinal chemistry for building complex heterocyclic systems with potential antimicrobial and kinase inhibitory activities. Also utilized in research settings to develop fluorescent probes, leveraging the inherent photophysical properties of the quinoline core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿4,000.00
inventory 1g
10-20 days ฿9,190.00

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ethyl 4-hydroxy-6-methoxy-8-methylquinoline-3-carboxylate
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of reactive functional groups—hydroxy, methoxy, and ester—that allow for further chemical modifications. Commonly employed in medicinal chemistry for building complex heterocyclic systems with potential antimicrobial and kinase inhibitory activities. Also utilized in research settings to develo

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of reactive functional groups—hydroxy, methoxy, and ester—that allow for further chemical modifications. Commonly employed in medicinal chemistry for building complex heterocyclic systems with potential antimicrobial and kinase inhibitory activities. Also utilized in research settings to develop fluorescent probes, leveraging the inherent photophysical properties of the quinoline core.

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