Ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate

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Reagent Code: #185278
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CAS Number 449197-54-0

science Other reagents with same CAS 449197-54-0

blur_circular Chemical Specifications

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Weight 439.23 g/mol
Formula C₁₉H₁₄BrF₃N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design potent and selective drug candidates, especially in oncology and inflammatory disease areas. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its modifiable functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,530.00
inventory 250mg
10-20 days ฿7,450.00
inventory 1g
10-20 days ฿24,020.00

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Ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design potent and selective drug candidates, especially in oncology and inflammatory disease areas. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its modifiable functional grou

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets involved in cell signaling pathways. Commonly employed in research settings to design potent and selective drug candidates, especially in oncology and inflammatory disease areas. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its modifiable functional groups.

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