2-(Trifluoromethyl)benzenesulfonyl Chloride

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Reagent Code: #240499
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CAS Number 776-04-5

science Other reagents with same CAS 776-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.61 g/mol
Formula C₇H₄ClF₃O₂S
thermostat Physical Properties
Boiling Point 133-135°C 14mm Hg (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Widely used in organic synthesis as a sulfonylating agent, particularly in the preparation of sulfonamides, which are key motifs in pharmaceuticals and agrochemicals. It reacts readily with amines to form sulfonamide derivatives, enabling the development of bioactive molecules. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability of the resulting products. Commonly employed in medicinal chemistry for structure–activity relationship studies and in the synthesis of functional materials. Also utilized as an intermediate in the production of dyes, polymers, and specialty chemicals where enhanced lipophilicity and metabolic stability are desired.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿690.00
inventory 25g
10-20 days ฿2,450.00
inventory 100g
10-20 days ฿9,350.00

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2-(Trifluoromethyl)benzenesulfonyl Chloride
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Widely used in organic synthesis as a sulfonylating agent, particularly in the preparation of sulfonamides, which are key motifs in pharmaceuticals and agrochemicals. It reacts readily with amines to form sulfonamide derivatives, enabling the development of bioactive molecules. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability of the resulting products. Commonly employed in medicinal chemistry for structure–activity relationship studies and in the synthesis of functional ma

Widely used in organic synthesis as a sulfonylating agent, particularly in the preparation of sulfonamides, which are key motifs in pharmaceuticals and agrochemicals. It reacts readily with amines to form sulfonamide derivatives, enabling the development of bioactive molecules. Its electron-withdrawing trifluoromethyl group enhances reactivity and stability of the resulting products. Commonly employed in medicinal chemistry for structure–activity relationship studies and in the synthesis of functional materials. Also utilized as an intermediate in the production of dyes, polymers, and specialty chemicals where enhanced lipophilicity and metabolic stability are desired.

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