Ethyl 4-chloro-5-(trifluoromethyl)quinoline-3-carboxylate

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Reagent Code: #124278
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CAS Number 2177266-12-3

science Other reagents with same CAS 2177266-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.66 g/mol
Formula C₁₃H₉ClF₃NO₂
badge Registry Numbers
MDL Number MFCD31629653
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the creation of quinoline-based compounds, which are explored for their potential therapeutic applications, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting drugs, making it a crucial component in medicinal chemistry. Researchers also utilize it in the design of novel agrochemicals, leveraging its structural features to develop pesticides and herbicides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,673.00
inventory 100mg
10-20 days ฿12,168.00

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Ethyl 4-chloro-5-(trifluoromethyl)quinoline-3-carboxylate
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the creation of quinoline-based compounds, which are explored for their potential therapeutic applications, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting drugs, making it a crucial component i

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. It is particularly valuable in the creation of quinoline-based compounds, which are explored for their potential therapeutic applications, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting drugs, making it a crucial component in medicinal chemistry. Researchers also utilize it in the design of novel agrochemicals, leveraging its structural features to develop pesticides and herbicides with improved efficacy and selectivity.

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