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Chemical Structure| 4837-90-5 Chemical Structure| 4837-90-5
Chemical Structure| 4837-90-5

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Product Details of 4-Methoxyindole

CAS No. :4837-90-5
Formula : C9H9NO
M.W : 147.17
SMILES Code : C1=C[NH]C2=C1C(=CC=C2)OC
MDL No. :MFCD00009737

Safety of 4-Methoxyindole

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 4-Methoxyindole

* 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 [ 4837-90-5 ]

[ 4837-90-5 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 22630-08-6 ]
  • [ 4837-88-1 ]
  • [ 4837-90-5 ]
  • 2
  • [ 4837-88-1 ]
  • [ 4637-24-5 ]
  • [ 4837-90-5 ]
  • 3
  • [ 4837-90-5 ]
  • [ 26638-43-7 ]
  • 2-(4-methoxy-indole-1-sulfonyl)-benzoic acid methyl ester [ No CAS ]
  • 5
  • [ 4837-90-5 ]
  • [ 406938-53-2 ]
  • 6
  • [ 112970-44-2 ]
  • [ 4837-90-5 ]
  • 7
  • [ 4837-90-5 ]
  • [ 14135-38-7 ]
  • [ 530116-20-2 ]
YieldReaction ConditionsOperation in experiment
85% Compound 1 (3 g, 0.026 mol) was dissolved in DMF (150 mL), and cooled to 0° C. NaH (dry, 95percent, 0.97 g, 0.038 mol) was added, and the reaction was stirred for 15 min. A solution of 2-fluorophenyl disulphide (6.5 g, 0.026 mol) in DMF (5 mL) was added, and the reaction was allowed to proceed at r.t. overnight. The reaction was quenched with H2O. Solvent was removed. CH2Cl2 was added to dilution the reaction mixture. The organics were extracted with brine (50 ml.x.2) and H2O (50 ml.x.2). The organic layer was dried over Na2SO4 and concentrated to dryness. The crude product was purified via (10percent EtOAc/hexanes) to give 5.33 g (85percent) of compound 2 as a white solid.
  • 9
  • [ 4837-90-5 ]
  • [ 3471-31-6 ]
  • 5-methoxy-3-((4-methoxy-1H-indol-3-yl)methyl)-1H-indole [ No CAS ]
 

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