4'-Bromo-2,2,2-trifluoroacetophenone

98%

Reagent Code: #144369
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CAS Number 16184-89-7

science Other reagents with same CAS 16184-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.02 g/mol
Formula C₈H₄BrF₃O
badge Registry Numbers
MDL Number MFCD00191862
inventory_2 Storage & Handling
Storage Room temperature, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug compounds where the trifluoromethyl group enhances metabolic stability and bioavailability. Its bromo functionality allows for further cross-coupling reactions, making it valuable in building complex organic molecules, especially in medicinal chemistry and agrochemical research. Commonly employed in Suzuki and other palladium-catalyzed reactions to form carbon-carbon bonds. Also utilized in the preparation of chiral catalysts and functional materials due to its reactive and structurally distinct features.

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Test Parameter Specification
Purity 97.5-100
Melting Point (°C) 26-31°C
Appearance Colorless to light yellow liquid or solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿990.00
inventory 25g
10-20 days ฿4,770.00
inventory 100g
10-20 days ฿14,000.00
inventory 1g
10-20 days ฿180.00
4'-Bromo-2,2,2-trifluoroacetophenone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug compounds where the trifluoromethyl group enhances metabolic stability and bioavailability. Its bromo functionality allows for further cross-coupling reactions, making it valuable in building complex organic molecules, especially in medicinal chemistry and agrochemical research. Commonly employed in Suzuki and other palladium-catalyzed reactions to form carbon-carbon bonds. Also utilized in

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug compounds where the trifluoromethyl group enhances metabolic stability and bioavailability. Its bromo functionality allows for further cross-coupling reactions, making it valuable in building complex organic molecules, especially in medicinal chemistry and agrochemical research. Commonly employed in Suzuki and other palladium-catalyzed reactions to form carbon-carbon bonds. Also utilized in the preparation of chiral catalysts and functional materials due to its reactive and structurally distinct features.

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