5-Bromo-2-Trifluoromethylbenzoic Acid

≥98%

Reagent Code: #147183
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CAS Number 654-97-7

science Other reagents with same CAS 654-97-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.02 g/mol
Formula C₈H₄BrF₃O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring halogenated aromatic structures. Its bromo and trifluoromethyl functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of fungicides, herbicides, and anti-inflammatory agents. Also utilized in research for designing novel compounds with enhanced metabolic stability and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿990.00
1g
10-20 days ฿2,290.00
5g
10-20 days ฿8,950.00
10g
10-20 days ฿16,440.00
25g
10-20 days ฿33,210.00
5-Bromo-2-Trifluoromethylbenzoic Acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring halogenated aromatic structures. Its bromo and trifluoromethyl functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of fungicides, herbicides, and anti-inflammatory agents. Also utilized in research for designing novel compounds with enhanced m

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients requiring halogenated aromatic structures. Its bromo and trifluoromethyl functional groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of fungicides, herbicides, and anti-inflammatory agents. Also utilized in research for designing novel compounds with enhanced metabolic stability and binding affinity.

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