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Chemical Structure| 3770-50-1 Chemical Structure| 3770-50-1
Chemical Structure| 3770-50-1

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Synonyms: 2-Carbethoxyindole; 2-Ethoxycarbonylindole

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Product Details of Ethyl indole-2-carboxylate

CAS No. :3770-50-1
Formula : C11H11NO2
M.W : 189.21
SMILES Code : C1=C(C(OCC)=O)[NH]C2=C1C=CC=C2
Synonyms :
2-Carbethoxyindole; 2-Ethoxycarbonylindole
MDL No. :MFCD00005609
InChI Key :QQXQAEWRSVZPJM-UHFFFAOYSA-N
Pubchem ID :73125

Safety of Ethyl indole-2-carboxylate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of Ethyl indole-2-carboxylate

* 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 [ 3770-50-1 ]

[ 3770-50-1 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 3770-50-1 ]
  • [ 6414-69-3 ]
  • [ 63158-53-2 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In acetonitrile; EXAMPLE VI Ethyl 2-Carboethoxy-3-indolepropanoate Ethyl 2-indolecarboxylate (3 gm), <strong>[6414-69-3]ethyl 3-iodopropanoate</strong> (5.4 gm), potassium carbonate (5 gm), and acetonitrile (50 ml) were combined and the mixture heated to reflux for 48 hours. The mixture was cooled and poured into water (50 ml). The mixture was extracted with ether (3*75 ml) and the combined ether extracts were washed with water (3*30 ml). The organic layer was dried over sodium sulfate and the solvent removed on a rotary evaporator. The diester product was obtained as a colorless oil.
  • 2
  • [ 3770-50-1 ]
  • [ 16932-45-9 ]
  • [ 131157-33-0 ]
  • 4
  • [ 79-37-8 ]
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  • [ 64-17-5 ]
  • [ 127221-02-7 ]
  • [ 128942-88-1 ]
  • 5
  • [ 3770-50-1 ]
  • [ 1700-31-8 ]
  • [ 915700-93-5 ]
  • 6
  • [ 3770-50-1 ]
  • [ 85482-13-9 ]
  • [ 915700-96-8 ]
  • 7
  • [ 3770-50-1 ]
  • [ 13920-91-7 ]
  • [ 1000069-56-6 ]
  • 10
  • [ 3770-50-1 ]
  • [ 2632-14-6 ]
  • [ 1049318-37-7 ]
 

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