98141-54-9

Upstream product

• 95-82-9 2,5 dichloroaniline 
• 608-31-1 2,6-Dichloroaniline 
• 17700-54-8 2,6-dichloroacetanilide 

Downstream Products

• 152134-99-1 4-Amino-N-[1-((4-amino-3-nitro-phenyl)-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-3,5-dichlorobenzenesulphonamide 
• 608-31-1 2,6-Dichloroaniline 
• 1191030-55-3 2-(4-amino-3,5-dichloro-benzenesulfonylamino)-4-(2-cyano-pyrrol-1-yl)-N-methoxy-N-methyl-butyramide 
• 1191030-43-9 2-(4-amino-3,5-dichloro-benzenesulfonylamino)-4-(2-nitro-imidazol-1-yl)-butyric acid 
• 1191030-46-2 2-(4-amino-3,5-dichloro-benzenesulfonylamino)-4-(2-cyano-pyrrol-1-yl)-butyric acid 
• 1191030-42-8 2-(4-amino-3,5-dichloro-benzenesulfonylamino)-4-(2-chloro-imidazol-1-yl)-butyric acid methyl ester 
• 1191030-44-0 2-(4-amino-3,5-dichloro-benzenesulfonylamino)-4-1,2,3-triazol-2-yl-butyric acid 
• 1191031-85-2 4-amino-3,5-dichloro-N-{3-(2-chloro-1H-imidazol-1-yl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 
• 1191031-71-6 4-amino-3,5-dichloro-N-{3-(2-cyano-1H-imidazol-1-yl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 
• 1191031-97-6 4-amino-3,5-dichloro-N-{1-[(4-methylpiperidini-1-yl)carbonyl]-3-(2-nitro-1H-imidazol-1-yl)propyl}benzenesulfonamide 
• 1191031-67-0 4-amino-3,5-dichloro-N-{3-(2-cyano-1H-pyrrol-1-yl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 
• 1191032-67-3 4-amino-3,5-dichloro-N-{3-(5-chloro-1H-pyrazol-1-yl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 
• 1191031-72-7 4-amino-3,5-dichloro-N-{3-(5-cyano-1H-pyrazol-1-yl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 
• 1198055-28-5 4-amino-3,5-dichloro-N-{3-(2-chlorophenyl)-1-[(4-methylpiperidin-1-yl)carbonyl]propyl}benzenesulfonamide 

Relevant academic research and scientific papers

2-SULFONYLAMINO-4-HETEROARYL BUTYRAMIDE ANTAGONISTS OF CCR10

This invention relates to a compound of formula (I) and the pharmaceutically acceptable salts thereof wherein R1, R2, R4. Ar and Het are as defined herein. The invention also relates to methods of using the compound of for

Monoazo dyes which are free from water-solubilizing groups and which contain a fluorosulphonyl group and process for colouring polyamides and polyester materials therewith

A process for coloring a synthetic textile material or fibre blend thereof which comprises applying to the synthetic textile material a compound or mixture thereof, which is free from water solubilizing groups, of Formula (1): wherein A and D each independently is an optionally substituted heterocyclic or carbocyclic group and at least one of A or D carries directly at least one --SO2 F group or carries a substituent to which at least one --SO2 F group is attached except for 4-(4-fluorosulphonylphenylazo)-N,N-dimethylaniline, provided that one of A or D is not 3,5-difluorosulphonylthien-2-yl, optionally substituted 1-phenyl-pyrazol-4-yl-5-one or STR1 or that one of A or D does not carry an --NCH2 CH(OH)CH2 Cl, --NCOCH2 Cl or --NCH2 CH2 SO2 F substituent. The presence of one or more --SO2 F groups in a dye molecule generally improves the properties of that dye and confers surprisingly good wet fastness and light fastness properties.