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N,N-Dimethylsulfamide

Basic information Safety Supplier Related

N,N-Dimethylsulfamide Basic information

Product Name:
N,N-Dimethylsulfamide
Synonyms:
  • dimethylsulfamide
  • N,N-DIMETHYLSULFAMIDE
  • N,N-DIMETHYLSULFAMOYLAMIDE
  • [methyl(sulfamoyl)amino]methane
  • EOS-60610
  • N.N-DiMethylsu
  • N,N-Dimethylsulfamide>
  • Sulfamide, N,N-dimethyl-
CAS:
3984-14-3
MF:
C2H8N2O2S
MW:
124.16
Product Categories:
  • Aliphatics
  • Amines
  • Sulfur & Selenium Compounds
  • API intermediates
  • CHIRAL CHEMICALS
  • sulfonyl compound
Mol File:
3984-14-3.mol
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N,N-Dimethylsulfamide Chemical Properties

Melting point:
95-96
Boiling point:
216.9±23.0 °C(Predicted)
Density 
1.327±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Acetone (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
11.41±0.60(Predicted)
color 
White to Off-White
CAS DataBase Reference
3984-14-3(CAS DataBase Reference)
EPA Substance Registry System
Sulfamide, N,N-dimethyl- (3984-14-3)
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Safety Information

Safety Statements 
24/25
HS Code 
2935.90.9500
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N,N-Dimethylsulfamide Usage And Synthesis

Chemical Properties

White Solid

Uses

N,N-Dimethylsulfamide is a byproduct of Tolylfluanide (T536730) fungicide decomposition found in some waters. Upon ozonization it becomes a precursor for carcinogenic Nitrosodimethylamine (N525625). Otherwise N,N-Dimethylsulfamide is a versatile reactant used in various syntheses such as preparation of N-sulfonylbenzaldimines in copper-catalyzed aza-Friedel-Crafts reactions with 1-methylindole.

Synthesis

13360-57-1

3984-14-3

General procedure for the synthesis of N,N-dimethylsulfonamide from N,N-dimethylaminosulfonyl chloride: N,N-dimethylaminosulfonyl chloride (6.96 mmol, 0.748 mL) was reacted with a methanol solution of 7 N ammonia (104 mmol, 14.92 mL) in a sealed autoclave at 60°C for 16 hours. After completion of the reaction, the solvent was removed from the reaction mixture by evaporation. The resulting solid was suspended in dichloromethane (DCM), filtered and washed with DCM. Subsequently, it was dried under reduced pressure to afford N,N-dimethylsulfonamide (850 mg, yield: 98%), which could be used in subsequent steps without further purification. The product was characterized by 1H NMR (300 MHz, DMSO-d6) with chemical shifts of δ 7.40 (2H, s), 2.38 (6H, s).

References

[1] Patent: WO2013/149997, 2013, A1. Location in patent: Page/Page column 146; 147
[2] Patent: WO2013/102826, 2013, A1. Location in patent: Page/Page column 84
[3] Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1980, vol. 19, # 10, p. 935 - 937
[4] Tetrahedron Letters, 2009, vol. 50, # 19, p. 2232 - 2235
[5] Chemische Berichte, 1950, vol. 83, p. 551,554

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