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Chemical Structure| 18903-01-0 Chemical Structure| 18903-01-0

Structure of 18903-01-0

Chemical Structure| 18903-01-0

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Product Details of [ 18903-01-0 ]

CAS No. :18903-01-0
Formula : C13H18N2
M.W : 202.30
SMILES Code : N1(C/C=C/C2=CC=CC=C2)CCNCC1
MDL No. :MFCD00063251
InChI Key :WGEIOMTZIIOUMA-QPJJXVBHSA-N
Pubchem ID :726896

Safety of [ 18903-01-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 18903-01-0 ]

* 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 [ 18903-01-0 ]

[ 18903-01-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 18903-01-0 ]
  • [ 53052-06-5 ]
  • (E)-2-(4-cinnamylpiperazin-1-yl)oxazolo[4,5-b]pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% In toluene; at 150.0℃; for 16h; In a 100ml round bottom flask was placed 0.604g (4mmol) of benzoxazole and 0.688g (8 mmol) of anhydrouspiperazine or substituted piperazine derivative. 50 ml of drytoluene was added to this mixture and the contents werestirred and refluxed over an oil bath maintained at 150C for16-18 hours. After this period, the mixture was cooled andthe solvent was rotary evaporated and the residue wassubjected to column chromatography over silica gel usingmethanol/methylene chloride (20/80) to furnish the titledcompounds.
  • 2
  • [ 18903-01-0 ]
  • [ 53052-06-5 ]
  • (E)-2-(4-cinnamylpiperazin-1-yl)benzo[d]oxazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
64% In toluene; at 150.0℃; for 16h; In a 100ml round bottom flask was placed 0.604g (4mmol) of benzoxazole and 0.688g (8 mmol) of anhydrouspiperazine or substituted piperazine derivative. 50 ml of drytoluene was added to this mixture and the contents werestirred and refluxed over an oil bath maintained at 150C for16-18 hours. After this period, the mixture was cooled andthe solvent was rotary evaporated and the residue wassubjected to column chromatography over silica gel usingmethanol/methylene chloride (20/80) to furnish the titledcompounds.
 

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