Basic information Safety Supplier Related

1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE

Basic information Safety Supplier Related

1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE Basic information

Product Name:
1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE
Synonyms:
  • 1-PHENYLSULPHONYLINDOLE-3-CARBOXALDEHYDE
  • 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE
  • 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBOXALDEHYDE
  • 1-(PHENYLSULFONYL)-3-INDOLECARBOXALDEHYDE
  • 1-BENZENESULFONYL-1 H-INDOLE-3-CARBALDEHYDE
  • BUTTPARK 98\04-06
  • 3-Formyl-1-(phenylsulphonyl)-1H-indole
  • 1-(Benzenesulfonyl)indole-3-carboxaldehyde
CAS:
80360-20-9
MF:
C15H11NO3S
MW:
285.32
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
Mol File:
80360-20-9.mol
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1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE Chemical Properties

Melting point:
157-161 °C(lit.)
Boiling point:
513.6±42.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
Light yellow to brown Solid
CAS DataBase Reference
80360-20-9
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
HS Code 
2933998090

MSDS

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1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBALDEHYDE Usage And Synthesis

Synthesis

487-89-8

98-09-9

80360-20-9

GENERAL STEPS: NaH (60% dispersed in mineral oil, 40.00 mmol, 0.96 g) was added in batches to a stirred solution of 3-indolecarboxaldehyde (20.00 mmol, 2.90 g) in anhydrous THF (50 mL) under ice bath cooling conditions. After slowly warming to room temperature, stirring was continued for 30 min. Subsequently, anhydrous THF solution of benzenesulfonyl chloride (24.00 mmol, 4.24 g) was added dropwise. The progress of the reaction was monitored by TLC and after complete disappearance of the raw material 3-indolecarboxaldehyde, the solvent was removed by evaporation under reduced pressure. The reaction mixture was diluted with ice water (300 mL) and the solid product was collected by filtration. Recrystallization with acetone/petroleum ether (60-90 °C) afforded the target product 1-(phenylsulfonyl)-3-indolecarboxaldehyde in 97% yield, melting point 151-153 °C. 1H NMR (600 MHz, CDCl3): δ 7.37 (t, J = 7.2 Hz, 1H), 7.42 (dd, J = 11.4, 4.2 Hz, 1H), 7.52 (t, J = 7.8 Hz, 2H), 7.62 (t, J = 7.2 Hz, 1H), 7.97 (t, J = 7.8 Hz, 3H), 8.20-8.31 (m, 2H), 10.11 (s, 1H). HRMS (MALDI): m/z 286.0515. calculated value C15H11NO3S: [M + H]+ 286.0538.

References

[1] Synlett, 1999, # 6, p. 786 - 788
[2] European Journal of Medicinal Chemistry, 2012, vol. 53, p. 283 - 291
[3] Journal of Organic Chemistry, 2002, vol. 67, # 3, p. 1001 - 1003
[4] Synthetic Communications, 2007, vol. 37, # 5, p. 829 - 837
[5] Tetrahedron, 1998, vol. 54, # 46, p. 13915 - 13928

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