1-[3-nitro-5-(trifluoromethyl)phenyl]ethanone

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Reagent Code: #219475
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CAS Number 39174-87-3

science Other reagents with same CAS 39174-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.14 g/mol
Formula C₉H₆F₃NO₃
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MDL Number MFCD11847337
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a fluorinated aromatic scaffold. Its nitro and trifluoromethyl functional groups make it suitable for further chemical transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in research settings for designing compounds with potential antimicrobial, anti-inflammatory, or herbicidal activity. Also utilized in the preparation of specialty chemicals where electron-withdrawing substituents are needed to modulate reactivity or stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,200.00
inventory 250mg
10-20 days ฿14,800.00
inventory 1g
10-20 days ฿31,350.00

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1-[3-nitro-5-(trifluoromethyl)phenyl]ethanone
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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 fluorinated aromatic scaffold. Its nitro and trifluoromethyl functional groups make it suitable for further chemical transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in research settings for designing compounds with potential antimicrobial, anti-inflammatory, or herbicidal activity. Also utili

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require a fluorinated aromatic scaffold. Its nitro and trifluoromethyl functional groups make it suitable for further chemical transformations, such as reduction of the nitro group to an amine for use in coupling reactions. Commonly employed in research settings for designing compounds with potential antimicrobial, anti-inflammatory, or herbicidal activity. Also utilized in the preparation of specialty chemicals where electron-withdrawing substituents are needed to modulate reactivity or stability.

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