4-(5-Methyl-3-phenyl-4-isoxazolyl)benzenesulfonyl chloride

≥98%

Reagent Code: #207791
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CAS Number 509074-26-4

science Other reagents with same CAS 509074-26-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.79 g/mol
Formula C₁₆H₁₂ClNO₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of valdecoxib, a selective COX-2 inhibitor for treating osteoarthritis and rheumatoid arthritis. The reactive sulfonyl chloride group facilitates the formation of sulfonamides by reaction with amines, yielding potent anti-inflammatory agents with high specificity for the COX-2 enzyme. Widely employed in medicinal chemistry to develop non-steroidal anti-inflammatory drugs (NSAIDs) that reduce gastrointestinal side effects. The isoxazole moiety provides structural stability and enhances the selectivity and pharmacokinetic profile of the resulting pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,070.00
inventory 1g
10-20 days ฿2,660.00
inventory 5g
10-20 days ฿8,040.00

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4-(5-Methyl-3-phenyl-4-isoxazolyl)benzenesulfonyl chloride
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Used as a key intermediate in the synthesis of valdecoxib, a selective COX-2 inhibitor for treating osteoarthritis and rheumatoid arthritis. The reactive sulfonyl chloride group facilitates the formation of sulfonamides by reaction with amines, yielding potent anti-inflammatory agents with high specificity for the COX-2 enzyme. Widely employed in medicinal chemistry to develop non-steroidal anti-inflammatory drugs (NSAIDs) that reduce gastrointestinal side effects. The isoxazole moiety provides structura

Used as a key intermediate in the synthesis of valdecoxib, a selective COX-2 inhibitor for treating osteoarthritis and rheumatoid arthritis. The reactive sulfonyl chloride group facilitates the formation of sulfonamides by reaction with amines, yielding potent anti-inflammatory agents with high specificity for the COX-2 enzyme. Widely employed in medicinal chemistry to develop non-steroidal anti-inflammatory drugs (NSAIDs) that reduce gastrointestinal side effects. The isoxazole moiety provides structural stability and enhances the selectivity and pharmacokinetic profile of the resulting pharmaceuticals.

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