2-Bromo-3-(trifluoromethyl)benzoicacid

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Reagent Code: #155074
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CAS Number 177420-63-2

science Other reagents with same CAS 177420-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2692 g/mol
Formula C₈H₄BrF₃O₂
badge Registry Numbers
MDL Number MFCD08532493
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a brominated and trifluoromethylated aromatic scaffold. Its functional groups allow for further chemical modifications through cross-coupling reactions, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Also employed in the preparation of specialty chemicals where the combination of electron-withdrawing trifluoromethyl group and the reactive bromine site enhances reactivity and selectivity in organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿760.00
inventory 250mg
10-20 days ฿1,100.00
inventory 1g
10-20 days ฿3,480.00
inventory 5g
10-20 days ฿17,390.00
inventory 25g
10-20 days ฿81,390.00

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2-Bromo-3-(trifluoromethyl)benzoicacid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a brominated and trifluoromethylated aromatic scaffold. Its functional groups allow for further chemical modifications through cross-coupling reactions, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Also employed in the preparation of specialty chemicals where the combination of electron-withdrawing trifluoromethyl

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a brominated and trifluoromethylated aromatic scaffold. Its functional groups allow for further chemical modifications through cross-coupling reactions, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Also employed in the preparation of specialty chemicals where the combination of electron-withdrawing trifluoromethyl group and the reactive bromine site enhances reactivity and selectivity in organic transformations.

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