194044-54-7

Basic information

• Product Name: 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonami de
• Synonyms: 4-(5-(4-Methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide;Ccris 9330;Hsdb 7038;p-(5-p-Tolyl-3-(trifluoromethyl)pyrazol-1-yl)benzenesulfonamide
• CAS NO: 194044-54-7
• Molecular Formula: C17H14F3N3O2S
• Molecular Weight: 0
• Mol File: 194044-54-7.mol
• Article Data: 125

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonami de(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonami de(194044-54-7)
• EPA Substance Registry System: 4-[5-(4-methylphenyl)-3-(trifluoromethyl)pyrazol-1-yl]benzenesulfonami de(194044-54-7)

Safety Data

• Hazardous Substances Data: 194044-54-7(Hazardous Substances Data)

Upstream product

• 720-94-5 4,4,4-trifluoro-1-(4-methylphenyl)butane-1,3-dione 
• 17852-52-7 4-hydrazinobenzene-1-sulfonamide hydrochloride 
• 74-88-4 methyl iodide 
• 4392-54-5 4-aminosulfonylphenylhydrazine 
• 96107-01-6 (E)-1,1,1,-trifluoro-4-(p-tolyl)but-3-en-2-one 
• 383-63-1 ethyl trifluoroacetate, 
• 122-00-9 para-methylacetophenone 
• 1233497-39-6 C₂₆H₂₃F₃N₄O₃S 
• 5450-86-2 para-aminophenylsulfonyl hydrazide 
• 63-74-1 sulfanilamide 
• 55949-65-0 4-[1-(4-methylphenyl)vinyl]morpholine 
• 365530-13-8 4-[5-(4-methylphenyl)-3-trifluoromethyl-1H-pyrazol-1-yl]aniline 
• 100-16-3 4-nitrophenylhydrazone 
• 365530-10-5 5-(4-methylphenyl)-1-(4-nitrophenyl)-3-trifluoromethylpyrazole 

Downstream Products

• 1426535-47-8 C₂₆H₂₂F₃N₃O₃S 
• 1426535-45-6 C₂₆H₂₁F₃N₄O₅S 
• 1426535-43-4 C₂₅H₁₉F₃N₄O₅S 
• 1446354-68-2 N-[(4-trifluoromethylphenyl)carbamothioyl]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-69-3 N-(3-ethyl-4-oxo-1,3-thiazolidin-2-yldene)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-64-8 N-(ethylcarbamothioyl)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-65-9 N-(phenylcarbamothioyl)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-70-6 N-(3-phenyl-4-oxo-1,3-thiazolidin-2-yldene)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-66-0 N-(benzylcarbamothioyl)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-71-7 N-(3-benzyl-4-oxo-1,3-thiazolidin-2-yldene)-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-67-1 N-[(4-nitrophenyl)carbamothioyl]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 
• 1446354-72-8 N-[3-(4-nitrophenyl)-4-oxo-1,3-thiazolidin-2-yldene]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1Hpyrazol-1-yl]benzenesulfonamide 
• 1538558-30-3 (Z)-3,7-dimethyl-1,9-dioxo-1-(4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenylsulfonamido)-6,8,10-trioxa-3,4,5-triazadodec-4-ene 4-oxide 
• 1538558-24-5 (Z)-7-methyl-1,11-dioxo-1-phenyl-11-(4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenylsulfonamido)-2,4,10-trioxa-5,6,7-triazaundec-5-ene 6-oxide 

Relevant articles and documents

Rapid Access to N-Protected Sulfonimidoyl Fluorides: Divergent Synthesis of Sulfonamides and Sulfonimidamides

Herein we report a practical and efficient copper-catalyzed approach for the conversion of various arenediazonium salts to the corresponding N-protected sulfonimidoyl fluorides. This operationally simple protocol tolerates a wide range of functional groups and can be applied to the late-stage modification of complex bioactive molecules. Furthermore, pharmaceutically important primary sulfonamides and sulfonimidamides derived from these valuable N-protected sulfonimidoyl fluoride units were prepared in minimal synthetic steps.

Nickel(II)-Catalyzed Addition of Aryl and Heteroaryl Boroxines to the Sulfinylamine Reagent TrNSO: The Catalytic Synthesis of Sulfinamides, Sulfonimidamides, and Primary Sulfonamides

We report a redox-neutral Ni(II)-catalyzed addition of (hetero)aryl boroxines to N-sulfinyltritylamine (TrNSO). The reactions use a catalyst generated from the combination of commercial, air-stable NiCl2·(glyme) and a commercially available bipyridine lig

A CONTINUOUS FLOW MICRO-TOTAL PROCESS SYSTEM FOR PREPARATION OF CELECOXIB AND ANALOGS THEREOF

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