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Chemical Structure| 13636-53-8 Chemical Structure| 13636-53-8

Structure of 13636-53-8

Chemical Structure| 13636-53-8

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Product Details of [ 13636-53-8 ]

CAS No. :13636-53-8
Formula : C8H12N2
M.W : 136.19
SMILES Code : NNC1=CC=C(C)C(C)=C1
MDL No. :MFCD02656652
InChI Key :ACHREEHAAAECOR-UHFFFAOYSA-N
Pubchem ID :173741

Safety of [ 13636-53-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H319-H372-H410
Precautionary Statements:P501-P273-P260-P270-P264-P280-P391-P314-P337+P313-P305+P351+P338-P301+P312+P330
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 13636-53-8 ]

* 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 [ 13636-53-8 ]

[ 13636-53-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3314-30-5 ]
  • [ 13636-53-8 ]
  • (E)-2-((2-(3,4-dimethylphenyl)hydrazono)methyl)-1H-benzo[d]imidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
56.7% In methanol; at 20℃; for 2h; General procedure: The equimolar aldehyde 3a?3d (1 mmol) and substituted phenylhydrazine 5a?5s (1 mmol) weremixed in CH3OH (10 mL) and stirred at room temperature [18]. After about 2 h, the reaction wascompleted (monitored by TLC). The residual crude was purified via silica gel column chromatogramusing a gradient mixture of petroleum ether and ethyl acetate to obtain the pure target compounds6a?6ai (in 45?80percent yield).
  • 2
  • [ 3012-80-4 ]
  • [ 13636-53-8 ]
  • (E)-2-((2-(3,4-dimethylphenyl)hydrazineylidene)methyl)-1-methyl-1H-benzo[d]imidazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% 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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