1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethanone

≥95%

Reagent Code: #142857
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CAS Number 34773-51-8

science Other reagents with same CAS 34773-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₆H₂BrF₃OS
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MDL Number MFCD07380810
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and inflammatory diseases. Its structure supports cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The electron-withdrawing trifluoromethyl and bromine groups enhance its reactivity in metal-catalyzed transformations, enabling efficient derivatization in drug discovery pipelines.

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inventory 1g
10-20 days ฿5,170.00

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1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and inflammatory diseases. Its structure supports cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The electron-withdrawing trifluoromethyl and bromine groups enhan
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders and inflammatory diseases. Its structure supports cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The electron-withdrawing trifluoromethyl and bromine groups enhance its reactivity in metal-catalyzed transformations, enabling efficient derivatization in drug discovery pipelines.
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