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N-Methyl-2-nitrobenzenesulphonamide

Product Name
N-Methyl-2-nitrobenzenesulphonamide
CAS No.
23530-40-7
Chemical Name
N-Methyl-2-nitrobenzenesulphonamide
Synonyms
2-(N-Methylsulphamoyl)nitrobenzene;N-methyl-2-nitrobenzenesulfonamide;N-Methyl-2-nitrobenzenesulphonamide;BenzenesulfonaMide, N-Methyl-2-nitro-;N-methyl-2-nitrobenzene-1-sulfonamide;2-(N-Methylsulphamoyl)nitrobenzene, 2-[(Methylamino)sulphonyl]nitrobenzene
CBNumber
CB0957984
Molecular Formula
C7H8N2O4S
Formula Weight
216.21
MOL File
23530-40-7.mol
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N-Methyl-2-nitrobenzenesulphonamide Property

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

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2935909099
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TRC
Product number
M339285
Product name
N-Methyl-2-nitrobenzenesulfonamide
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
M339285
Product name
N-Methyl-2-nitrobenzenesulfonamide
Packaging
50mg
Price
$60
Updated
2021/12/16
ChemScene
Product number
CS-M2486
Product name
Benzenesulfonamide,N-methyl-2-nitro-
Purity
99.45%
Packaging
1g
Price
$51
Updated
2021/12/16
Matrix Scientific
Product number
046907
Product name
N-Methyl-2-nitrobenzenesulfonamide
Purity
>95%
Packaging
1g
Price
$79
Updated
2021/12/16
SynQuest Laboratories
Product number
8669-1-X2
Product name
N-Methyl-2-nitrobenzenesulfonamide
Packaging
1g
Price
$92
Updated
2021/12/16
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N-Methyl-2-nitrobenzenesulphonamide Chemical Properties,Usage,Production

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

N-Methyl-2-nitrobenzenesulphonamide Preparation Products And Raw materials

Raw materials

Preparation Products

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N-Methyl-2-nitrobenzenesulphonamide Suppliers

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