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Chemical Structure| 27372-41-4 Chemical Structure| 27372-41-4

Structure of 27372-41-4

Chemical Structure| 27372-41-4

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Product Details of [ 27372-41-4 ]

CAS No. :27372-41-4
Formula : C12H12BrN
M.W : 250.13
SMILES Code : BrC1=CC=CC2=C1NC3=C2CCCC3
MDL No. :MFCD08272271

Safety of [ 27372-41-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 27372-41-4 ]

* 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 [ 27372-41-4 ]

[ 27372-41-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 16732-66-4 ]
  • [ 27372-41-4 ]
  • 2
  • [ 108-94-1 ]
  • [ 16732-66-4 ]
  • [ 27372-41-4 ]
YieldReaction ConditionsOperation in experiment
13.1 g With acetic acid; at 130℃; for 12h; 16 g (85.8 mmol) of Intermediate 1-4 and 8.4 g (85.8 mmol) of cyclohexanone were dissolved in 100 mL of acetic acid, and the reaction mixture was heated at about 130 C. under reflux for about 12 hours. After completion of the reaction, the solvent was removed to obtain a solid product, which was extracted with ethylacetate. The combined organic extracts were dried with magnesium sulfate to remove moisture, and the product was separated and purified by column chromatography to obtain about 13.1 g (52.3 mmol, Yield: 61%) of Intermediate 1-3. This compound was identified by LC-MS. 16 g (85.8 mmol) of Intermediate 1-4 and 8.4 g (85.8 mmol) of cyclohexanone were dissolved in 100 mL of acetic acid, and the reaction mixture was heated at about 130 C. under reflux for about 12 hours. After completion of the reaction, the solvent was removed to obtain a solid product, which was extracted with ethylacetate. The combined organic extracts were dried with magnesium sulfate to remove moisture, and the product was separated and purified by column chromatography to obtain about 13.1 g (52.3 mmol, Yield: 61%) of Intermediate 1-3. This compound was identified by LC-MS. LC-MS m/z=250.02 (M+H)+
  • 3
  • [ 27372-41-4 ]
  • [ 132906-53-7 ]
 

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