4-[4-(TRIFLUOROMETHYL)PHENYL]BENZENESULFONYL CHLORIDE

95%

Reagent Code: #244890
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CAS Number 524046-23-9

science Other reagents with same CAS 524046-23-9

blur_circular Chemical Specifications

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Weight 320.71 g/mol
Formula C₁₃H₈ClF₃O₂S
badge Registry Numbers
MDL Number MFCD01631923
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antitumor agents. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in medicinal chemistry for modifying drug candidates to enhance metabolic stability and binding affinity. Also utilized in the preparation of functionalized polymers and liquid crystals due to its rigid aromatic structure and electron-withdrawing trifluoromethyl group.

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inventory 250mg
10-20 days ฿11,680.00

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4-[4-(TRIFLUOROMETHYL)PHENYL]BENZENESULFONYL CHLORIDE
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antitumor agents. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in medicinal chemistry for modifying drug candidates to enhance metabolic stability and binding affinity. Also utilized in the preparation of functionalized polymers and liquid crystals due to its rigid

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antitumor agents. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in medicinal chemistry for modifying drug candidates to enhance metabolic stability and binding affinity. Also utilized in the preparation of functionalized polymers and liquid crystals due to its rigid aromatic structure and electron-withdrawing trifluoromethyl group.

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