Basic information Safety Supplier Related

Isopropylsulfonamide

Basic information Safety Supplier Related

Isopropylsulfonamide Basic information

Product Name:
Isopropylsulfonamide
Synonyms:
  • propane-2-sulfonamide
  • IsopropylsulfonamidePropane-2-sulfonamide
  • Isopropylsulfonamide
  • Propane-2-sulphonamide, 2-Sulphamoylpropane
  • 2-Propanesulfonamide
  • Isopropylsulphonamide 98%
  • 2-Propanesulfonamide (9CI, ACI)
  • Propan-2-sulfonamide
CAS:
81363-76-0
MF:
C3H9NO2S
MW:
123.17
Product Categories:
  • CHIRAL CHEMICALS
Mol File:
81363-76-0.mol
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Isopropylsulfonamide Chemical Properties

Melting point:
61-65 °C(Solv: chloroform (67-66-3); carbon tetrachloride (56-23-5))
Boiling point:
216.5±23.0 °C(Predicted)
Density 
1.194±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
10.69±0.60(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C3H9NO2S/c1-3(2)7(4,5)6/h3H,1-2H3,(H2,4,5,6)
InChIKey
SJMCLWCCNYAWRQ-UHFFFAOYSA-N
SMILES
CC(S(N)(=O)=O)C
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Safety Information

HS Code 
2935909099
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Isopropylsulfonamide Usage And Synthesis

Chemical Properties

Type of white solid

Synthesis

10147-37-2

81363-76-0

The general procedure for the synthesis of isopropylsulfonamide from isopropylsulfonyl chloride is as follows: 500 μL of isopropylsulfonyl chloride (4.5 mmol) was slowly added to a mixture of 6 mL of methylene chloride and 11 mL of ammonium hydroxide at room temperature. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the organic layer was separated by extraction with dichloromethane. The organic layer was dried with anhydrous magnesium sulfate, the desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure to give 121 mg of isopropylsulfonamide in 22% yield. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 1.4 (d, J = 6.8 Hz, 6H), 3.2 (m, 1H), 4.4 (s, 2H).

References

[1] Patent: EP514133, 1992, A1
[2] Patent: US5428031, 1995, A
[3] Journal of Fluorine Chemistry, 1996, vol. 79, # 1, p. 71 - 75
[4] Patent: US2005/143422, 2005, A1. Location in patent: Page/Page column 52
[5] Recueil des Travaux Chimiques des Pays-Bas, 1906, vol. 25, p. 215

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