4-Bromo-2-(trifluoromethyl)quinoline-3-carboxylic acid

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Reagent Code: #150698
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CAS Number 587886-11-1

science Other reagents with same CAS 587886-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.06 g/mol
Formula C₁₁H₅BrF₃NO₂
badge Registry Numbers
MDL Number MFCD08458126
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure supports the formation of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry for constructing quinoline-based scaffolds that exhibit antiviral and anticancer activities. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing groups and stable aromatic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,510.00
inventory 250mg
10-20 days ฿5,980.00
inventory 1g
10-20 days ฿22,720.00

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4-Bromo-2-(trifluoromethyl)quinoline-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure supports the formation of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry for constructing quinoline-based scaffolds that exhibit antiviral and anticancer activities. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing groups and stable aromatic fra

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its structure supports the formation of bioactive molecules with high selectivity and potency. Commonly employed in medicinal chemistry for constructing quinoline-based scaffolds that exhibit antiviral and anticancer activities. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing groups and stable aromatic framework.

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