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Chemical Structure| 136918-66-6 Chemical Structure| 136918-66-6

Structure of 136918-66-6

Chemical Structure| 136918-66-6

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Product Details of [ 136918-66-6 ]

CAS No. :136918-66-6
Formula : C14H14ClNO3
M.W : 279.72
SMILES Code : O=CC(C1=O)=C(Cl)C2=C(O1)C=C(N(CC)CC)C=C2
MDL No. :MFCD00232978
InChI Key :CYXXVTLWYIGJJW-UHFFFAOYSA-N
Pubchem ID :2828082

Safety of [ 136918-66-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 136918-66-6 ]

* 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 [ 136918-66-6 ]

[ 136918-66-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 136918-66-6 ]
  • [ 175883-62-2 ]
  • KSH-V-38 [ No CAS ]
  • 2
  • [ 619-60-3 ]
  • [ 136918-66-6 ]
  • C22H24N2O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With triethylamine; In acetonitrile; at 80℃; for 4h;Inert atmosphere; 4-chloro-3-aldehyde-7-diethylaminocoumarin (reference numeral 1,1mmol, 279mg) was dissolved in 5mL anhydrous acetonitrile (acetonitrile), followed by addition of 4-dimethylaminopyridine phenoxide acid (1mmol, 173mg), and finally added triethylamine (NEt33) (1mmol, 139muL) as a base, an argon atmosphere, 80 deg.] C the reaction was refluxed for 4h, rotary evaporation, to obtain a mixture, and the mixture was purified to give Compound A, wherein the mixture is a red-brown solid, was purified to give a dark brown compound A, a total of 304mg yield 80percent;The main compound in the product mixture A;
  • 3
  • [ 619-60-3 ]
  • [ 136918-66-6 ]
  • C25H24N4O3 [ No CAS ]
 

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