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Chemical Structure| 56448-22-7 Chemical Structure| 56448-22-7

Structure of 56448-22-7

Chemical Structure| 56448-22-7

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Product Details of [ 56448-22-7 ]

CAS No. :56448-22-7
Formula : C11H9NO
M.W : 171.20
SMILES Code : O=CC1=CNC(C2=CC=CC=C2)=C1
MDL No. :MFCD11875829
InChI Key :CXRIBBUJKKGAGS-UHFFFAOYSA-N
Pubchem ID :11052090

Safety of [ 56448-22-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501

Application In Synthesis of [ 56448-22-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 56448-22-7 ]

[ 56448-22-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 56448-22-7 ]
  • [ 42899-76-3 ]
  • [ 881676-90-0 ]
YieldReaction ConditionsOperation in experiment
75% Reference Example 234 5-Phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde Under an argon atmosphere, 5-phenyl-1H-pyrrole-3-carbaldehyde (342 mg) was dissolved in absolute tetrahydrofuran (20 mL) and sodium hydride (60percent in oil, 240 mg) was added while stirring at room temperature. After stirring at the same temperature for 15 min, 15-crown-5 (1.21 mL) was added, and the mixture was further stirred at the same temperature for 15 min. Pyridin-3-ylsulfonyl chloride hydrochloride (642 mg) was added, and the mixture was further stirred at the same temperature for 30 min. The reaction mixture was diluted with ethyl acetate, washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1?1:1) to give the title compound as a brown solid (yield 470 mg, 75percent). 1H-NMR (CDCl3)delta: 6.60 (1H, d, J=1.8 Hz), 7.15-7.19 (2H, m), 7.25-7.37 (3H, m), 7.42-7.48 (1H, m), 7.53-7.57 (1H, m), 8.13 (1H, d, J=1.8 Hz), 8.49-8.50 (1H, m), 8.74-8.76 (1H, m), 9.90 (1H, s).
In tetrahydrofuran; Reference Example 234 5-Phenyl-1-(pyridin-3-ylsulfonyl)-1H-pyrrole-3-carbaldehyde Under an argon atmosphere, 5-phenyl-1H-pyrrole-3-carbaldehyde (342 mg) was dissolved in absolute tetrahydrofuran (20 mL) and sodium hydride (60percent in oil, 240 mg) was added while stirring at room temperature. After stirring at the same temperature for 15 min, 15-crown-5 (1.21 mL) was added, and the mixture was further stirred at the same temperature for 15 min. Pyridin-3-ylsulfonyl chloride hydrochloride (642 mg) was added, and the mixture was further stirred at the same temperature for 30 min. The reaction mixture was diluted with ethyl acetate, washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=19:1-->1:1) to give the title compound as a brown solid (yield 470 mg, 75percent). 1H-NMR (CDCl3)delta: 6.60 (1H, d, J=1.8 Hz), 7.15-7.19 (2H, m), 7.25-7.37 (3H, m), 7.42-7.48 (1H, m), 7.53-7.57 (1H, m), 8.13 (1H, d, J=1.8 Hz), 8.49-8.50 (1H, m), 8.74-8.76 (1H, m), 9.90 (1H, s).
  • 2
  • [ 56448-22-7 ]
  • [ 26638-43-7 ]
  • [ 881676-65-9 ]
YieldReaction ConditionsOperation in experiment
Reference Example 224 Methyl 2-[(4-formyl-2-phenyl-1H-pyrrol-1-yl)sulfonyl]benzoate Using 5-phenyl-1H-pyrrole-3-carbaldehyde (513 mg), sodium hydride (60% in oil, 216 mg), 15-crown-5 (990 mg) and <strong>[26638-43-7]methyl 2-(chlorosulfonyl)benzoate</strong> (1.06 g), a procedure as in Reference Example 219 was performed to give the title compound as a pale-yellow oil (yield 664 mg, 60%). 1H-NMR (CDCl3)delta: 3.88 (3H, s), 6.59 (1H, d, J=1. Hz), 7.07 (1H, d, J=7.2 Hz), 7.14-7.26 (5H, m), 7.33-7.36 (1H, m), 7.56-7.58 (2H, m), 8.11 (1H, d, J=1.8 Hz), 9.92 (1H, s).
 

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