2-Chloro-6-(trifluoromethyl)quinoline

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Reagent Code: #124085
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CAS Number 78060-56-7

science Other reagents with same CAS 78060-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.6 g/mol
Formula C₁₀H₅ClF₃N
badge Registry Numbers
MDL Number MFCD09029680
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various drugs, particularly those targeting infectious diseases and inflammation. Its quinoline core structure is often incorporated into molecules designed to inhibit specific enzymes or receptors, enhancing therapeutic efficacy.

In agrochemicals, it is employed in the development of pesticides and herbicides. The trifluoromethyl group enhances the compound's ability to interact with biological targets in pests and weeds, improving its effectiveness as a crop protection agent. Additionally, its chemical stability and reactivity make it a valuable building block in organic synthesis for creating more complex molecules with specific biological activities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,620.00
inventory 100mg
10-20 days ฿6,255.00
inventory 1g
10-20 days ฿28,665.00

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2-Chloro-6-(trifluoromethyl)quinoline
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This compound is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various drugs, particularly those targeting infectious diseases and inflammation. Its quinoline core structure is often incorporated into molecules designed to inhibit specific enzymes or receptors, enhancing therapeutic efficacy.

In agrochemicals, it is employed in the development of pesticides and her

This compound is primarily utilized in the pharmaceutical and agrochemical industries due to its unique structural properties. In pharmaceuticals, it serves as a key intermediate in the synthesis of various drugs, particularly those targeting infectious diseases and inflammation. Its quinoline core structure is often incorporated into molecules designed to inhibit specific enzymes or receptors, enhancing therapeutic efficacy.

In agrochemicals, it is employed in the development of pesticides and herbicides. The trifluoromethyl group enhances the compound's ability to interact with biological targets in pests and weeds, improving its effectiveness as a crop protection agent. Additionally, its chemical stability and reactivity make it a valuable building block in organic synthesis for creating more complex molecules with specific biological activities.

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