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Chemical Structure| 2700-22-3 Chemical Structure| 2700-22-3

Structure of 2700-22-3

Chemical Structure| 2700-22-3

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Product Details of [ 2700-22-3 ]

CAS No. :2700-22-3
Formula : C10H6N2
M.W : 154.17
SMILES Code : N#C/C(C#N)=C/C1=CC=CC=C1
MDL No. :MFCD00001855
InChI Key :WAVNYPVYNSIHNC-UHFFFAOYSA-N
Pubchem ID :17608

Safety of [ 2700-22-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302+H312+H332-H315-H319-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 2700-22-3 ]

* 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 [ 2700-22-3 ]

[ 2700-22-3 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 28710-97-6 ]
  • [ 2700-22-3 ]
  • [ 141987-80-6 ]
  • 3
  • [ 2700-22-3 ]
  • [ 4596-92-3 ]
  • 2-Amino-6-chloro-1-oxy-quinoline-3-carbonitrile [ No CAS ]
  • 4
  • [ 27037-34-9 ]
  • [ 2700-22-3 ]
  • [ 405296-92-6 ]
  • 5
  • [ 2700-22-3 ]
  • [ 4273-92-1 ]
  • 3-amino-2-cyano-1-phenyl-1<i>H</i>-benzo[<i>f</i>]chromene-5-carboxylic acid (4-chloro-2,5-dimethoxy-phenyl)-amide [ No CAS ]
  • 6
  • [ 2700-22-3 ]
  • [ 102831-44-7 ]
  • [ 1314080-63-1 ]
  • 8
  • [ 2700-22-3 ]
  • [ 145091-87-8 ]
  • [ 81000-11-5 ]
YieldReaction ConditionsOperation in experiment
57% General procedure: Dichloromethane (10 mL) was taken in a round-bottomed flask,into which 1.0 equivalent (1 mmol) of triethylamine and pyrazolonewere poured. The mixture was stirred for 2 min without heating. To this mixture, 1.0 equivalent of corresponding presynthesized benzylidene from malononitrile was added. Then the mixture was agitated for 25-30 min. The reaction was observed by TLC. The desired products appeared as precipitates. The precipitates were washed with water to remove the unreacted pyrazolone to obtain pure products. Melting points were recordedfor crystalline substances.
 

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