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.

Available Sizes & Pricing

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