Basic information Safety Supplier Related

3-DIMETHYLSULFAMOYL-BENZOIC ACID

Basic information Safety Supplier Related

3-DIMETHYLSULFAMOYL-BENZOIC ACID Basic information

Product Name:
3-DIMETHYLSULFAMOYL-BENZOIC ACID
Synonyms:
  • 3-(Dimethylsulphamoyl)benzoic acid
  • 3-[(Dimethylamino)sulphonyl]benzoic acid
  • 3-(N,N-DiMethylsulfaMoyl)benzoic acid
  • Benzoic acid, 3-[(diMethylaMino)sulfonyl]-
  • 3-(N,N-Dimethylsulphamoyl)benzoic acid
  • 3-[(Dimethylamino)sulphonyl]benzoic acid, 3-Carboxy-N,N-dimethylbenzenesulphonamide
  • 3-[(dimethylamino)sulfonyl]benzenecarboxylic acid
CAS:
7326-73-0
MF:
C9H11NO4S
MW:
229.25
Mol File:
7326-73-0.mol
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3-DIMETHYLSULFAMOYL-BENZOIC ACID Chemical Properties

Melting point:
174-176°
Boiling point:
417.1±47.0 °C(Predicted)
Density 
1.368±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.69±0.10(Predicted)
form 
solid
color 
Off white
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Safety Information

HazardClass 
IRRITANT
HS Code 
2935909099
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3-DIMETHYLSULFAMOYL-BENZOIC ACID Usage And Synthesis

Uses

3-Dimethylsulfamoylbenzoic acid

Synthesis

4025-64-3

124-40-3

7326-73-0

The general procedure for the synthesis of N,N-dimethyl-3-carboxybenzenesulfonamide from 3-chlorosulfonylbenzoic acid and dimethylamine was as follows: 3-chlorosulfonylbenzoic acid (2.60 g, 12 mmol) was dissolved in dichloromethane (DCM, 20 mL), followed by the addition of dimethylamine (2.0 M in tetrahydrofuran (THF), 20 mL, 40 mmol, 3.3 equiv). The reaction mixture was stirred at room temperature for 30 min before the reaction was quenched with 10% hydrochloric acid (HCl) solution. The reaction mixture was extracted with ethyl acetate (EtOAc) and the organic phase was washed with saturated sodium chloride (NaCl) solution and dried with anhydrous sodium sulfate (Na2SO4). Finally, the organic solvent was removed by distillation under reduced pressure to afford the target product N,N-dimethyl-3-carboxybenzenesulfonamide (1.80 g, 65% yield); mass spectrum (m/z) 229.

References

[1] ChemMedChem, 2015, vol. 10, # 9, p. 1548 - 1558
[2] Patent: WO2006/24834, 2006, A1. Location in patent: Page/Page column 82
[3] Patent: WO2006/24836, 2006, A1. Location in patent: Page/Page column 30
[4] Patent: WO2007/71963, 2007, A2. Location in patent: Page/Page column 50
[5] Patent: WO2006/40568, 2006, A1. Location in patent: Page/Page column 82

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