2,4,5-trifluorobenzene-1-sulfonyl chloride

≥98%

Reagent Code: #240273
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CAS Number 220227-21-4

science Other reagents with same CAS 220227-21-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.59 g/mol
Formula C₆H₂ClF₃O₂S
badge Registry Numbers
MDL Number MFCD00077600
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a sulfonylation reagent in organic synthesis, particularly in the preparation of sulfonamides and sulfonate esters. Its fluorinated aromatic ring enhances reactivity and influences the electronic properties of the final products, making it valuable in pharmaceutical and agrochemical development. Commonly employed in the synthesis of bioactive molecules where fluorine substitution improves metabolic stability and binding affinity. Also utilized in materials science for modifying polymer properties or building fluorinated functional materials. The compound’s selectivity and reactivity profile make it suitable for constructing complex molecules in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,110.00
inventory 10g
10-20 days ฿2,060.00
inventory 100g
10-20 days ฿14,980.00
inventory 500g
10-20 days ฿65,010.00
inventory 25g
10-20 days ฿4,320.00
2,4,5-trifluorobenzene-1-sulfonyl chloride
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Widely used as a sulfonylation reagent in organic synthesis, particularly in the preparation of sulfonamides and sulfonate esters. Its fluorinated aromatic ring enhances reactivity and influences the electronic properties of the final products, making it valuable in pharmaceutical and agrochemical development. Commonly employed in the synthesis of bioactive molecules where fluorine substitution improves metabolic stability and binding affinity. Also utilized in materials science for modifying polymer pro

Widely used as a sulfonylation reagent in organic synthesis, particularly in the preparation of sulfonamides and sulfonate esters. Its fluorinated aromatic ring enhances reactivity and influences the electronic properties of the final products, making it valuable in pharmaceutical and agrochemical development. Commonly employed in the synthesis of bioactive molecules where fluorine substitution improves metabolic stability and binding affinity. Also utilized in materials science for modifying polymer properties or building fluorinated functional materials. The compound’s selectivity and reactivity profile make it suitable for constructing complex molecules in medicinal chemistry research.

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