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Chemical Structure| 51145-58-5 Chemical Structure| 51145-58-5

Structure of 51145-58-5

Chemical Structure| 51145-58-5

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Product Details of [ 51145-58-5 ]

CAS No. :51145-58-5
Formula : C13H14N2O
M.W : 214.26
SMILES Code : NNC1=CC=C(OCC2=CC=CC=C2)C=C1
MDL No. :MFCD01993592
InChI Key :UFZKWTITXBRSPK-UHFFFAOYSA-N
Pubchem ID :561392

Safety of [ 51145-58-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of [ 51145-58-5 ]

* 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 [ 51145-58-5 ]

[ 51145-58-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3012-80-4 ]
  • [ 51145-58-5 ]
  • (E)-2-((2-(4-(benzyloxy)phenyl)hydrazineylidene)methyl)-1-methyl-1H-benzo[d]imidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
94% In ethanol; at 20℃; for 4h; General procedure: The hydrazones 1-10 were prepared by a condensation reaction between phenylhydrazine derivatives and imidazole or benzimidazole carbaldehydes [45-47]. In a 25-mL Erlenmeyer flask, 1mmol of 1-methylbenzimidazole-2-carbaldehyde or 1-methylimidazole-2-carbaldehyde and 1mmol of phenylhydrazine derivative (phenylhydrazine, 4-methoxyphenylhydrazine, 3,4-dimethylphenylhydrazine, 4-chlorophenylhydrazine and (4-benzylphenyl)hydrazine) were dissolved in 3ml of ethanol. The reaction mixture was stirred at room temperature for 4h, and then filtered and air-dried. The resulting residue was then purified by recrystallization in a mixture of ethanol/DMSO to give the pure product.
 

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