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[ CAS No. 13278-67-6 ] {[proInfo.proName]}

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Chemical Structure| 13278-67-6
Chemical Structure| 13278-67-6
Structure of 13278-67-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13278-67-6 ]

CAS No. :13278-67-6 MDL No. :MFCD00041302
Formula : C8H11N3S Boiling Point : -
Linear Structure Formula :- InChI Key :IEAWRKQVDLFINI-UHFFFAOYSA-N
M.W : 181.26 Pubchem ID :737132
Synonyms :

Safety of [ 13278-67-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P501-P270-P264-P301+P310+P330-P405 UN#:2811
Hazard Statements:H301 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13278-67-6 ]

* 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 [ 13278-67-6 ]

[ 13278-67-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 25365-71-3 ]
  • [ 13278-67-6 ]
  • (E)-1-((2-phenyl-1H-indol-3-yl)methylene)-4-(p-tolyl)thiosemicarbazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% With acetic acid; In ethanol;Reflux; General procedure: The substituted 2-arylindole-3-carbaldehyde derivative 5a-g (1 mmol) and a few drops of acetic acid were added to a solution of substituted thiosemicarbazide derivative 2 (1.2 mmol) in ethanol (10 mL) . The mixture was stirred at reflux for 1-3 h and then cooled to room temperature. Then the solid separated was filtered and recrystallized from the mixture of ethyl acetate and n-hexane to give compounds 6a-p.
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