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[ CAS No. 5391-74-2 ] {[proInfo.proName]}

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Chemical Structure| 5391-74-2
Chemical Structure| 5391-74-2
Structure of 5391-74-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 5391-74-2 ]

CAS No. :5391-74-2 MDL No. :MFCD00026242
Formula : C9H10N2O Boiling Point : -
Linear Structure Formula :C6H5NHNCHC(O)CH3 InChI Key :-
M.W : 162.19 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 5391-74-2 ]

* 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 [ 5391-74-2 ]

[ 5391-74-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 62009-47-6 ]
  • [ 5391-74-2 ]
  • 4-methyl-1H-imidazole-2-carboxamide [ No CAS ]
  • 2
  • [ 2759-28-6 ]
  • [ 116026-94-9 ]
  • [ 5391-74-2 ]
  • 4-benzyl-N-{3-[1-(4-benzylpiperazin-1-yl)-3-oxo-2-(phenylhydrazono)butyl]pyridin-2-yl}piperazine-1-carboxamide [ No CAS ]
  • 3
  • [ 2826-25-7 ]
  • [ 5391-74-2 ]
  • [ 1253181-54-2 ]
YieldReaction ConditionsOperation in experiment
85% With pyridine In ethanol for 1.5h; Reflux; 6-Acetyl-3-amino-2-phenyl-5-(p-tolyl)-2,5-dihydropyridazine-4-carbonitrile (3f) General procedure: Pyridine (0.5 mL) was added to a mixture of 1-(2-phenylhydrazono)propan-2-one 1 (10 mmol, 1.62 g) and the appropriatebenzylidenemalononitrile derivative 2a-g (10 mmol) in ethanol(20 mL). The mixture was refluxed for 1.5 h and monitored by TLCusing n-hexane : ethyl acetate (2 : 1). After the completion of thereaction, the solvent was evaporated under reduced pressure andthe resulting crude product was washed with water (2 × 20 mL) andrecrystallised from ethanol
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