2,3,4,5-tetrafluorobenzoyl chloride

≥97%

Reagent Code: #240134
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CAS Number 94695-48-4

science Other reagents with same CAS 94695-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.53 g/mol
Formula C₇HClF₄O
badge Registry Numbers
MDL Number MFCD00075164
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the introduction of a tetrafluorobenzoyl group into larger molecules. Its high reactivity makes it valuable in forming amide and ester derivatives, especially in the development of fluorinated active ingredients. The presence of multiple fluorine atoms enhances metabolic stability and lipophilicity in target compounds, which is advantageous in drug design. It is also employed in the preparation of specialty polymers and liquid crystals where fluorination improves thermal and chemical resistance. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions in controlled environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿390.00
inventory 25g
10-20 days ฿590.00
inventory 100g
10-20 days ฿1,800.00
inventory 500g
10-20 days ฿8,680.00
2,3,4,5-tetrafluorobenzoyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the introduction of a tetrafluorobenzoyl group into larger molecules. Its high reactivity makes it valuable in forming amide and ester derivatives, especially in the development of fluorinated active ingredients. The presence of multiple fluorine atoms enhances metabolic stability and lipophilicity in target compounds, which is advantageous in drug design. It is also employed in the preparati

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound enables the introduction of a tetrafluorobenzoyl group into larger molecules. Its high reactivity makes it valuable in forming amide and ester derivatives, especially in the development of fluorinated active ingredients. The presence of multiple fluorine atoms enhances metabolic stability and lipophilicity in target compounds, which is advantageous in drug design. It is also employed in the preparation of specialty polymers and liquid crystals where fluorination improves thermal and chemical resistance. Due to its sensitivity to moisture, it is typically handled under anhydrous conditions in controlled environments.

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