Basic information Safety Supplier Related

N-Methyl-2-nitrobenzenesulphonamide

Basic information Safety Supplier Related

N-Methyl-2-nitrobenzenesulphonamide Basic information

Product Name:
N-Methyl-2-nitrobenzenesulphonamide
Synonyms:
  • N-Methyl-2-nitrobenzenesulphonamide
  • N-methyl-2-nitrobenzenesulfonamide
  • 2-(N-Methylsulphamoyl)nitrobenzene
  • BenzenesulfonaMide, N-Methyl-2-nitro-
  • 2-(N-Methylsulphamoyl)nitrobenzene, 2-[(Methylamino)sulphonyl]nitrobenzene
  • N-methyl-2-nitrobenzene-1-sulfonamide
CAS:
23530-40-7
MF:
C7H8N2O4S
MW:
216.21
Mol File:
23530-40-7.mol
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N-Methyl-2-nitrobenzenesulphonamide Chemical Properties

Melting point:
109-111
Boiling point:
378.6±44.0 °C(Predicted)
Density 
1.423±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
10.60±0.10(Predicted)
Appearance
White to yellow Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2935909099
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N-Methyl-2-nitrobenzenesulphonamide Usage And Synthesis

Synthesis

1694-92-4

74-89-5

23530-40-7

Step 2. Synthesis of N-methyl-2-nitrobenzenesulfonamide 2-Nitrobenzene-1-sulfonyl chloride (4 g, 18.05 mmol) was dissolved in dichloromethane (DCM, 60.2 mL) and cooled to 0 °C in an ice water bath. Subsequently, triethylamine (TEA, 7.55 mL, 54.1 mmol) and tetrahydrofuran solution of 2M methylamine (13.54 mL, 27.1 mmol) were added sequentially to this solution. The reaction mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction mixture was diluted with dichloromethane and washed with saturated aqueous sodium bicarbonate (NaHCO3) solution (2 x 100 mL) followed by brine (100 mL). The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. Finally, the concentrate was ground in ether to give N-methyl-2-nitrobenzenesulfonamide (3.12 g, 14.44 mmol, 80% yield). The product was analyzed by liquid chromatography-mass spectrometry (LCMS), showing a m/z of 217.1 (MH+) and a retention time of 0.53 min.

References

[1] Journal of Medicinal Chemistry, 2013, vol. 56, # 5, p. 2160 - 2164
[2] Patent: WO2012/92880, 2012, A1. Location in patent: Page/Page column 63-64
[3] Angewandte Chemie - International Edition, 2010, vol. 49, # 29, p. 4955 - 4957
[4] Chemical Communications, 2014, vol. 50, # 62, p. 8586 - 8589
[5] Patent: US9242996, 2016, B2. Location in patent: Page/Page column 255; 256

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