3-(Trifluoromethoxy)Benzenesulfonyl Chloride

98%

Reagent Code: #241114
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CAS Number 220227-84-9

science Other reagents with same CAS 220227-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.62 g/mol
Formula C₇H₄ClF₃O₃S
thermostat Physical Properties
Boiling Point 229-230 °C
inventory_2 Storage & Handling
Density 1.53g/mL
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—key motifs in drug design. It is also employed in the development of functional materials and specialty chemicals where the trifluoromethoxy group enhances lipophilicity and metabolic stability. Commonly utilized in research settings for building blocks in medicinal chemistry due to its reactivity and ability to introduce fluorinated aromatic segments into target molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿132.00
inventory 5g
10-20 days ฿341.00
inventory 25g
10-20 days ฿1,474.00
3-(Trifluoromethoxy)Benzenesulfonyl Chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—key motifs in drug design. It is also employed in the development of functional materials and specialty chemicals where the trifluoromethoxy group enhances lipophilicity and metabolic stability. Commonly utilized in research settings for building blocks in medicinal chemistry due

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—key motifs in drug design. It is also employed in the development of functional materials and specialty chemicals where the trifluoromethoxy group enhances lipophilicity and metabolic stability. Commonly utilized in research settings for building blocks in medicinal chemistry due to its reactivity and ability to introduce fluorinated aromatic segments into target molecules.

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