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Chemical Structure| 5448-47-5 Chemical Structure| 5448-47-5

Structure of 5448-47-5

Chemical Structure| 5448-47-5

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Product Details of [ 5448-47-5 ]

CAS No. :5448-47-5
Formula : C10H11N3O
M.W : 189.21
SMILES Code : O=C(NN)CC1=CNC2=C1C=CC=C2
MDL No. :MFCD00005634
InChI Key :GYHLCXMCGCVVCG-UHFFFAOYSA-N
Pubchem ID :21589

Safety of [ 5448-47-5 ]

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

Application In Synthesis of [ 5448-47-5 ]

* 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 [ 5448-47-5 ]

[ 5448-47-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 41042-12-0 ]
  • [ 5448-47-5 ]
  • 2-(1H-indol-3-yl)-N0-(2-oxo-1-propylindolin-3-ylidene)acetohydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% With acetic acid; In ethanol; for 2h;Reflux; General procedure: To a hot stirred solution of key intermediate 1H-indole-2-carbohydrazide 5 (0.18 gm, 1 mmoL) inabsolute ethyl alcohol (7 mL) and glacial acetic acid (catalytic amount), the appropriate N-unsubstituted1H-indole-2,3-dione 6a-f, N-substituted 1H-indole-2,3-dione 8a-h, or 1-tetralone 10 (1 mmoL) wasadded. The resulting mixture was refluxed for 2 hours, and then the formed solid was filtered owhile hot, washed with cold isopropyl alcohol, dried and recrystallized from DMF to aord targetbis-indoles (7a-f and 9a-h), and 11, respectively.
 

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Related Functional Groups of
[ 5448-47-5 ]

Amides

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Hydrazides

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Amines

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Hydrazines

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Related Parent Nucleus of
[ 5448-47-5 ]

Indoles

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