2-Bromo-6-(trifluoromethyl)benzoic acid

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Reagent Code: #146502
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CAS Number 177420-64-3

science Other reagents with same CAS 177420-64-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.02 g/mol
Formula C₈H₄BrF₃O₂
thermostat Physical Properties
Melting Point 134-138°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require fluorinated aromatic structures for enhanced metabolic stability and bioavailability. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules via palladium-catalyzed reactions such as Suzuki or Heck couplings. Commonly employed in research and development of new drug candidates, especially in anti-inflammatory, antifungal, and central nervous system agents. Also utilized in the preparation of liquid crystals and specialty polymers where halogenated, fluorinated building blocks are needed for specific electronic or thermal properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,730.00
inventory 10g
10-20 days ฿12,850.00
inventory 5g
10-20 days ฿6,420.00

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2-Bromo-6-(trifluoromethyl)benzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require fluorinated aromatic structures for enhanced metabolic stability and bioavailability. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules via palladium-catalyzed reactions such as Suzuki or Heck couplings. Commonly employed in research and development of new drug candi

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients that require fluorinated aromatic structures for enhanced metabolic stability and bioavailability. Its bromo and trifluoromethyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules via palladium-catalyzed reactions such as Suzuki or Heck couplings. Commonly employed in research and development of new drug candidates, especially in anti-inflammatory, antifungal, and central nervous system agents. Also utilized in the preparation of liquid crystals and specialty polymers where halogenated, fluorinated building blocks are needed for specific electronic or thermal properties.

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