80-20-6

Usage

Uses

Used in Dye and Pigment Production:
2-Aminophenol-4-sulfonanilide is utilized as a key intermediate in the synthesis of various dyes and pigments. Its chemical structure allows for the creation of a wide range of colorants used in different industries, including textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Aminophenol-4-sulfonanilide serves as a precursor for the development of new drugs. Its potential anti-cancer properties have been a subject of research, indicating its use as a compound in the discovery and synthesis of novel therapeutic agents.
Used in Organic Chemistry as a Reagent:
2-Aminophenol-4-sulfonanilide is employed as a reagent in various organic chemistry reactions. Its unique functional groups facilitate specific chemical transformations, making it a valuable tool in the synthesis of other important chemicals.
Used as a Precursor in Chemical Synthesis:
Beyond its direct applications, 2-Aminophenol-4-sulfonanilide also acts as a precursor for the synthesis of other significant chemicals. Its presence in the chemical library is crucial for the advancement of chemical research and the development of new materials and compounds.

InChI:InChI=1/C6H8N2O3S/c7-5-3-4(12(8,10)11)1-2-6(5)9/h1-3,9H,7H2,(H2,8,10,11)

Upstream product

• 98-37-3 2-aminophenol-4-sulfonic acid 
• 85879-78-3 4-acetoxy-3-acetylamino-benzenesulfonyl chloride 
• 62-53-3 aniline 
• 616-85-3 4-hydroxy-3-nitrobenzene sulfonic acid 
• 95-55-6 2-amino-phenol 

Downstream Products

• 122531-58-2 N,N'-Bis-(5-benzenesulfonylamino-2-hydroxy-phenyl)-succinamide 
• 122531-59-3 Hexanedioic acid bis-[(5-benzenesulfonylamino-2-hydroxy-phenyl)-amide] 
• 122531-69-5 C₃₇H₂₆Cl₂N₄O₁₀S₄ 
• 122531-62-8 C₃₇H₂₈N₄O₁₀S₄ 
• 122531-68-4 Butane-1,4-disulfonic acid bis-[(5-benzenesulfonylamino-3-chloro-2-hydroxy-phenyl)-amide] 
• 122531-70-8 Butane-1,4-disulfonic acid bis-({3-[(Z)-benzenesulfonylimino]-5-chloro-6-oxo-cyclohexa-1,4-dienyl}-amide) 
• 122531-63-9 Butane-1,4-disulfonic acid bis-({3-[(E)-benzenesulfonylimino]-6-oxo-cyclohexa-1,4-dienyl}-amide) 
• 122531-72-0 Hexanedioic acid bis-({3-[(Z)-benzenesulfonylimino]-5-chloro-6-oxo-cyclohexa-1,4-dienyl}-amide) 
• 122531-66-2 Decanedioic acid bis-({3-[(E)-benzenesulfonylimino]-6-oxo-cyclohexa-1,4-dienyl}-amide) 
• 122531-71-9 N,N'-Bis-{3-[(Z)-benzenesulfonylimino]-5-chloro-6-oxo-cyclohexa-1,4-dienyl}-succinamide 
• 122531-65-1 Hexanedioic acid bis-({3-[(E)-benzenesulfonylimino]-6-oxo-cyclohexa-1,4-dienyl}-amide) 
• 122531-64-0 N,N'-Bis-{3-[(E)-benzenesulfonylimino]-6-oxo-cyclohexa-1,4-dienyl}-succinamide 
• 111726-09-1 N-phenylsulfonyl-2,3-dichloro-6-phenylsulfonylamino-1,4-benzoquinone imine 
• 122531-74-2 N-{3-[(E)-Benzenesulfonylimino]-2,4,5-trichloro-6-oxo-cyclohexa-1,4-dienyl}-benzamide 

Relevant academic research and scientific papers

Unsymmetrical 1:2-chromium complexes containing an azo compound and an azomethine compound

Compounds of the formula: STR1 WHICH ARE EMINENTLY SUITABLE FOR DYEING NATURAL AND SYNTHETIC POLYAMIDES AND FOR COLORING SURFACE COATINGS. Dyeings on textile material are distinguished by very good lightfastness and very good fastness to wet treatments, for example fastness to water, perspiration, sea water and washing.

Metallized phenyl-azo-naphthol compounds

Metallized azo dyes of the formula STR1 wherein A is a sulfonyl, sulfonamido or carboxamido group, D is the residue of a phenol or naphthol, E is the residue of acetoacetanilide, a phenyl or naphthyl pyrazolone or the residue of a naphthol and M is a cation. The dyes are suitable for dyeing natural and synthetic polyamides, demonstrating good all-around fastness properties.