Basic information Safety Supplier Related

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE

Basic information Safety Supplier Related

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Basic information

Product Name:
N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE
Synonyms:
  • AURORA 2940
  • N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE
  • N-(4-ethanoylphenyl)methanesulfonamide
  • N-(4-Acetylphenyl)
  • Methanesulfonamide, N-(4-acetylphenyl)-
  • 4'-Acetylmethanesulfonanilide
  • 4'-ACETYLMETHANESULFONANILIDE
CAS:
5317-89-5
MF:
C9H11NO3S
MW:
213.25
Mol File:
5317-89-5.mol
More
Less

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Chemical Properties

Melting point:
150-152 °C
Boiling point:
369.4±44.0 °C(Predicted)
Density 
1.320±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
7.16±0.10(Predicted)
Appearance
White to light yellow Solid
More
Less

Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
More
Less

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Usage And Synthesis

Synthesis

99-92-3

124-63-0

5317-89-5

Cooled 4-aminoacetophenone (10 mmol) was dissolved in pyridine (10 mL) at 0 °C and methanesulfonyl chloride (15 mmol) was added slowly. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was diluted with H2O and extracted with ethyl acetate (EtOAc) several times. The organic layers were combined, washed sequentially with H2O and saturated brine and dried over anhydrous magnesium sulfate (MgSO4). After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by rapid column chromatography on silica gel, the eluent being a mixed solvent of ethyl acetate:hexane to afford N-(4-acetylphenyl)methanesulfonamide (Compound 13-5, LJO-298). The yield was 95% and the melting point was 161 °C. 1H NMR (CDCl3) δ: 7.97 (dd, 2H, J = 2.0, 6.8 Hz), 7.26 (dd, 2H, J = 2.0, 6.8 Hz), 6.87 (bs, 1H), 3.10 (s, 3H), 2.59 (s, 3H).

References

[1] Journal of Enzyme Inhibition and Medicinal Chemistry, 2014, vol. 29, # 6, p. 846 - 867
[2] Organic Process Research and Development, 1998, vol. 2, # 2, p. 71 - 77
[3] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 18, p. 6043 - 6053
[4] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 12, p. 2685 - 2688
[5] Patent: WO2005/3084, 2005, A1. Location in patent: Page 79

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDESupplier

Nanjing Chalf-Pharm Technology Co., Ltd.
Tel
025-57018978 18251899859
Email
sales@chalf-pharm.com
Cool Pharm, Ltd
Tel
021-60455363 18019463053
Email
sales@coolpharm.com
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Email
xg01_gj@163.com
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Email
3008007409@qq.com
Shanghai Chaolan Chemical Technology Center
Tel
021-QQ:65489617 15618227136
Email
Sales@ATKchemical.com