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Chemical Structure| 956-04-7 Chemical Structure| 956-04-7

Structure of 956-04-7

Chemical Structure| 956-04-7

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Product Details of [ 956-04-7 ]

CAS No. :956-04-7
Formula : C15H11ClO
M.W : 242.70
SMILES Code : O=C(C1=CC=CC=C1)/C=C/C2=CC=C(Cl)C=C2
MDL No. :MFCD00016345
InChI Key :ABGIIXRNMHUKII-DHZHZOJOSA-N
Pubchem ID :5377022

Safety of [ 956-04-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 956-04-7 ]

* 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 [ 956-04-7 ]

[ 956-04-7 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 956-04-7 ]
  • [ 20101-92-2 ]
  • [ 95734-12-6 ]
  • 2
  • [ 956-04-7 ]
  • [ 34800-90-3 ]
  • [ 70284-66-1 ]
  • 3
  • [ 956-04-7 ]
  • [ 51175-79-2 ]
  • [ 1138320-91-8 ]
  • 4
  • [ 956-04-7 ]
  • [ 4139-61-1 ]
  • [ 1450853-43-6 ]
YieldReaction ConditionsOperation in experiment
95% With iodine; acetic acid; at 100℃; for 0.916667h; General procedure: A mixture of a selected chalcone (0.5 mmol), 4-hydroxycoumarin (0.5 mmol),and iodine (0.5 mmol) was dissolved in 2-3mL acetic acid. Then, the mixture was stirred under reflux at 100 C for the time indicated in Table 1. The reaction mixture was cooled to room temperature and diluted with water, followed by Na2S2O3*H2O solution to quench excess iodine. The reaction mixture was filtered invacuo, and the residue was purified by column chromatography on silica gel (100-200mesh) usingh exane=EtOAc (10:2 to 10:1, v=v) as eluent to give the pure product.
  • 5
  • [ 956-04-7 ]
  • [ 78364-55-3 ]
  • 2-(5-(4-chlorophenyl)-4,5-dihydro-3-phenylpyrazol-1-yl)-6-fluorobenzo[d]thiazole [ No CAS ]
 

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Technical Information

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