6-(Trifluoromethyl)pyridine-3-sulfonyl chloride

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Reagent Code: #242370
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CAS Number 959996-58-8

science Other reagents with same CAS 959996-58-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.61 g/mol
Formula C₆H₃ClF₃NO₂S
badge Registry Numbers
MDL Number MFCD10699112
thermostat Physical Properties
Melting Point 40-45 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and insecticides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 6-(trifluoromethyl)pyridine moiety into larger molecules. This structural fragment is known to enhance metabolic stability and binding affinity in bioactive compounds. Commonly employed in the preparation of sulfonamide derivatives with biological activity. Also utilized in research settings for the design of novel catalysts and functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,490.00
inventory 1g
10-20 days ฿8,950.00
inventory 5g
10-20 days ฿28,450.00

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6-(Trifluoromethyl)pyridine-3-sulfonyl chloride
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and insecticides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 6-(trifluoromethyl)pyridine moiety into larger molecules. This structural fragment is known to enhance metabolic stability and binding affinity in bioactive compounds. Commonly employed in the preparation of sulfonamide derivatives with biological activit

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and insecticides. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for introducing the 6-(trifluoromethyl)pyridine moiety into larger molecules. This structural fragment is known to enhance metabolic stability and binding affinity in bioactive compounds. Commonly employed in the preparation of sulfonamide derivatives with biological activity. Also utilized in research settings for the design of novel catalysts and functional materials.

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