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Chemical Structure| 50262-46-9 Chemical Structure| 50262-46-9

Structure of 50262-46-9

Chemical Structure| 50262-46-9

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Product Details of [ 50262-46-9 ]

CAS No. :50262-46-9
Formula : C16H24O2
M.W : 248.36
SMILES Code : O=CC1=CC=C(OCCCCCCCCC)C=C1
MDL No. :MFCD00043712
Boiling Point : No data available

Safety of [ 50262-46-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 50262-46-9 ]

* 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 [ 50262-46-9 ]

[ 50262-46-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 50262-46-9 ]
  • [ 56621-89-7 ]
  • (2-Methoxy-pyrimidin-5-yl)-[1-(4-nonyloxy-phenyl)-meth-(E)-ylidene]-amine [ No CAS ]
  • 2
  • [ 50262-46-9 ]
  • [ 84-67-3 ]
  • [ 2416-12-8 ]
  • 3
  • [ 4318-78-9 ]
  • [ 50262-46-9 ]
  • C37H51N3O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With acetic acid; In ethanol; at 80℃; General procedure: This compound was synthesized by the method described in reference [18] for the synthesis of Schiff-base compounds. To a solution of <strong>[4318-78-9]3,5-diaminopyridine</strong> [IV] (0.01 mole) in absolute ethanol (10 mL) was added two molar amount of the 4-alkoxybenzaldhyde (0.02 mole) with two drops of glacial acetic acid and the mixture was refluxed at 80C for 5 hrs. After completion of reaction, the mixture was cooled and poured into the ice cold water. The solid obtained was filtered, washed with ice cold water, dried and recrystalized from ethanol.
 

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