Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Synthetic Anti-infective Drugs >  Sulfonamides and synergist >  4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE

4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE

Basic information Safety Supplier Related

4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE Basic information

Product Name:
4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE
Synonyms:
  • N,N-DIETHYL 4-BROMOBENZENESULFONAMIDE
  • 4-Bromo-N,N-diethylbenzenesulphonamide97%
  • 4-Bromo-N,N-diethylbenzenesulphonamide 97%
  • 4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE
  • 4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE USP/EP/BP
  • Benzenesulfonamide, 4-bromo-N,N-diethyl-
CAS:
90944-62-0
MF:
C10H14BrNO2S
MW:
292.19
Product Categories:
  • alkyl bromide
  • blocks
  • Bromides
  • Sulfonamides
Mol File:
90944-62-0.mol
More
Less

4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE Chemical Properties

Boiling point:
356.4±44.0 °C(Predicted)
Density 
1.431±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
-5.29±0.70(Predicted)
Appearance
Colorless to light yellow Liquid
More
Less

Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2935909099
More
Less

4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDE Usage And Synthesis

Synthesis

109-89-7

98-58-8

90944-62-0

4-Bromobenzenesulfonyl chloride (1.00 g, 3.91 mmol) was dissolved in dichloromethane (30.00 mL) and cooled in an ice bath. Diethylamine (1.19 mL, 11.54 mmol) was added slowly and dropwise to the reaction mixture, stirred for 5 minutes, then removed from the ice bath and stirring was continued for 12 hours at room temperature. After completion of the reaction, the reaction solution was concentrated under reduced pressure and the resulting residue was dissolved in dichloromethane and washed sequentially with water and saturated saline. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (n-hexane: ethyl acetate = 3:1) to afford the target compound 4-bromo-N,N-diethylbenzenesulfonamide (1.10 g, 96% yield).1H NMR (CDCl3, 500 MHz) δ 7.67 (4H, m), 3.23 (4H, q, J = 7.0 Hz), 1.13 (6H, t).

References

[1] Patent: EP3327000, 2018, A1. Location in patent: Paragraph 0102
[2] Journal of Medicinal Chemistry, 2000, vol. 43, # 21, p. 3878 - 3894
[3] Journal of the American Chemical Society, 1923, vol. 45, p. 2697
[4] Journal of Organic Chemistry, 2003, vol. 68, # 21, p. 8274 - 8276
[5] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 23, p. 6575 - 6577

4-BROMO-N,N-DIETHYLBENZENESULPHONAMIDESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Nanjing Norris-Pharm Technology Co., Ltd
Tel
18652989687
Email
sales@norris-pharm.com
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66113011 17798518460
Email
cfzhang@aikonchem.com