4-Chloro-3-nitrobenzenesulfonamide
4-Chloro-3-nitrobenzenesulfonamide Basic information
- Product Name:
- 4-Chloro-3-nitrobenzenesulfonamide
- Synonyms:
-
- BUTTPARK 76\07-88
- 3-NITRO-4-CHLOROBENZENESULFONAMIDE
- 4-CHLORO-3-NITROBENZENE-1-SULFONAMIDE
- 4-CHLORO-3-NITROBENZENESULFONAMIDE
- 4-CHLORO-3-NITROSULFAMYLBENZENE
- YELLOW SULFONE
- 4-chloro-3-nitro-benzenesulfonamid
- O-NITROCHLOROBENZENE-P-SULFONAMIDE
- CAS:
- 97-09-6
- MF:
- C6H5ClN2O4S
- MW:
- 236.63
- EINECS:
- 202-559-8
- Product Categories:
-
- Benzene derivates
- Intermediates of Dyes and Pigments
- Mol File:
- 97-09-6.mol
4-Chloro-3-nitrobenzenesulfonamide Chemical Properties
- Melting point:
- 25-35 °C
- Boiling point:
- 175-176 °C
- Density
- 1.5966 (rough estimate)
- refractive index
- 1.6000 (estimate)
- storage temp.
- Inert atmosphere,Room Temperature
- form
- crystalline powder
- pka
- 9.28±0.60(Predicted)
- color
- White to off white
- Water Solubility
- 224.8mg/L(15 ºC)
- CAS DataBase Reference
- 97-09-6(CAS DataBase Reference)
- EPA Substance Registry System
- Benzenesulfonamide, 4-chloro-3-nitro- (97-09-6)
Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HS Code
- 2935909099
- Hazardous Substances Data
- 97-09-6(Hazardous Substances Data)
4-Chloro-3-nitrobenzenesulfonamide Usage And Synthesis
Chemical Properties
Light yellow to light brown crystalline powder
Uses
4-Chloro-3-nitrobenzenesulfonamide is used as a chemical intermediate for azo dyes.
Synthesis
Chlorosulphonic acid (450 mL) was slowly added to 2-chloronitrobenzene (100 g). The reaction mass was heated to 100°C and maintained at that temperat ure for 6 hours before cooling to ambient temperature and stirring for an additional 12 hours. The reaction mass was slowly poured into chilled aqueous ammonia (800 mL) and the reaction mixture was stirred for 3 hours at -10°C. The reaction mixture was then warmed to 23°C and stirred for 2 h ours. The reaction mixture was then filtered and the obtained solid was washed three times with water (200 mL x 3). The solid was dissolved in methanol (600 mL) at 60°C, charged with water (200 mL), and was stirred for 1 hour at 60°C. Again, the reaction mixture was charged with water (200 mL) and stirred for 1 hour at 60°C. Once again, the reaction mixtu re was charged with water (200 mL) and stirred for 1 hour. After cooling to room temperature and stirring for 1 hour, the reaction mixture was filtered, and the solid was washed with a 1 :1 mixture of methanol and water (100 mL). The solid was dried under vacuum at 60°C. Crystallization of the residue with toluen e gave the 4-Chloro-3-nitrobenzenesulfonamide(50 g).
4-Chloro-3-nitrobenzenesulfonamide Preparation Products And Raw materials
Raw materials
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4-Chloro-3-nitrobenzenesulfonamide(97-09-6)Related Product Information
- Sodium 3-nitrobenzenesulphonate
- 4-Nitrophenyl chloroformate
- Epichlorohydrin
- 1-Chloro-3-nitrobenzene
- 2-Nitrochlorobenzene
- 3,4-Difluoronitrobenzene
- Sulfanilamide
- 3-Nitrobenzaldehyde
- p-Toluenesulfonamide
- chloronitrobenzene
- Chloroacetic acid
- 4-Chloronitrobenzene
- Difluorochloromethane
- 1,3-Dinitrobenzene
- 3-NITRO-4-CHLORO BENZENE SULFONANILIDE
- 2-NITROCHLOROBENZENE-4-(N,N-DIMETHYL)-SULPHONAMIDE
- 2-NITROCHLOROBENZENE-4-SULFOMETHYL AMIDE
- 2-CHLORO-5-NITROBENZENESULFONAMIDE 98%,2-CHLORO-5-NITROBENZENESULFONAMIDE