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Chemical Structure| 13156-95-1 Chemical Structure| 13156-95-1

Structure of 13156-95-1

Chemical Structure| 13156-95-1

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Product Details of [ 13156-95-1 ]

CAS No. :13156-95-1
Formula : C10H12ClNO
M.W : 197.66
SMILES Code : O=C(NCCC1=CC=CC=C1)CCl
MDL No. :MFCD00245084
InChI Key :LNWWGHNQLOXRTF-UHFFFAOYSA-N
Pubchem ID :94921

Safety of [ 13156-95-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 13156-95-1 ]

* 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 [ 13156-95-1 ]

[ 13156-95-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13156-95-1 ]
  • [ 13599-12-7 ]
  • [ 1357378-45-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In acetonitrile;Reflux; General procedure: A mixture of ethyl 3-aryl-1H-pyrazole-5-carboxylate 1 (2 mmol), N-aralkyl -2-chloroacetamide 7 (3 mmol), anhydrous potassium carbonate (4 mmol) and dry acetonitrile (60 ml) was refluxed for 1-5 h, after which the mixture was cooled to room temperature and filtered. The filtrate was condensed under reduced pressure. The crude product was purified by chromatographer on silica gel using PE/EtOAc (3:1) as an eluent to afford the desired compounds 5.
 

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