3-Fluoro-4-(trifluoromethyl)benzoyl chloride

95%

Reagent Code: #188335
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CAS Number 216144-68-2

science Other reagents with same CAS 216144-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.56 g/mol
Formula C₈H₃ClF₄O
badge Registry Numbers
MDL Number MFCD00236284
thermostat Physical Properties
Melting Point 152 °C
inventory_2 Storage & Handling
Density 1.486 g/mL at 25 °C (lit.)
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for the introduction of fluorinated aromatic moieties, which can enhance the bioavailability and metabolic stability of active compounds. Commonly employed in the production of herbicides and fungicides due to the electron-withdrawing properties of the trifluoromethyl and fluoro groups, which improve binding to biological targets. Also utilized in the preparation of specialty polymers and liquid crystals where fluorination contributes to thermal and chemical resistance. Reacts readily with nucleophiles such as amines and alcohols, making it valuable in constructing complex molecules through amide or ester formation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,050.00
5g
10-20 days ฿6,130.00
25g
10-20 days ฿29,830.00
250mg
10-20 days ฿1,270.00
3-Fluoro-4-(trifluoromethyl)benzoyl chloride
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its structure allows for the introduction of fluorinated aromatic moieties, which can enhance the bioavailability and metabolic stability of active compounds. Commonly employed in the production of herbicides and fungicides due to the electron-withdrawing properties of the trifluoromethyl and fluoro groups, which improve binding to biological targets. Also utilized in the preparation of specialty polymers and liquid crystals where fluorination contributes to thermal and chemical resistance. Reacts readily with nucleophiles such as amines and alcohols, making it valuable in constructing complex molecules through amide or ester formation.
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