3-(TRIFLUOROMETHYL)QUINOLINE-8-CARBOXYLIC ACID

≥95%

Reagent Code: #44448
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CAS Number 588702-66-3

science Other reagents with same CAS 588702-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.17 g/mol
Formula C₁₁H₆F₃NO₂
thermostat Physical Properties
Melting Point 182-185℃(decomp)(Solv: ethanol (64-17-5))
Boiling Point 379.6±37.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.481±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural features, including the trifluoromethyl group and quinoline core, make it valuable for developing compounds with potential biological activity. It is often employed in the creation of molecules targeting specific enzymes or receptors, particularly in the design of anti-inflammatory, antimicrobial, or anticancer drugs. Additionally, its carboxylic acid functionality allows for further chemical modifications, enabling the development of derivatives with enhanced pharmacological properties. Researchers also explore its use in organic synthesis to construct complex heterocyclic frameworks for drug discovery programs.

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inventory 1g
10-20 days ฿47,376.00

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3-(TRIFLUOROMETHYL)QUINOLINE-8-CARBOXYLIC ACID
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural features, including the trifluoromethyl group and quinoline core, make it valuable for developing compounds with potential biological activity. It is often employed in the creation of molecules targeting specific enzymes or receptors, particularly in the design of anti-inflammatory, antimicrobial, or anticancer drugs. Additionally, its carboxylic acid functionality allows for further chemical modifications, enabling the development of derivatives with enhanced pharmacological properties. Researchers also explore its use in organic synthesis to construct complex heterocyclic frameworks for drug discovery programs.
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