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[ CAS No. 53518-18-6 ] {[proInfo.proName]}

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Chemical Structure| 53518-18-6
Chemical Structure| 53518-18-6
Structure of 53518-18-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 53518-18-6 ]

CAS No. :53518-18-6 MDL No. :MFCD00041843
Formula : C16H14F3NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :VSSSHNJONFTXHS-UHFFFAOYSA-N
M.W : 309.28 Pubchem ID :72652
Synonyms :
Coumarin 540A

Safety of [ 53518-18-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 53518-18-6 ]

* 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 [ 53518-18-6 ]

[ 53518-18-6 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 336-64-1 ]
  • [ 53518-18-6 ]
  • [ 137516-28-0 ]
YieldReaction ConditionsOperation in experiment
26 % Turnov. In dichloromethane; 1,1,2-Trichloro-1,2,2-trifluoroethane for 4h; Heating;
  • 2
  • [ 53518-18-6 ]
  • β-cyclodextrin [ No CAS ]
  • C42H70O35*C16H14F3NO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water at 13.5 - 50℃; -ΔG;
YieldReaction ConditionsOperation in experiment
With poly (ethylene glycol) 6000; Tween 80 In water at 24.84℃;
  • 4
  • C116H96O32S8(8-)*8Na(1+) [ No CAS ]
  • [ 53518-18-6 ]
  • C116H96O32S8(8-)*8Na(1+)*C16H14F3NO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% In water at 20℃; for 1h;
  • 5
  • 4NO3(1-)*4C53H46N2O6*2Pt(2+) [ No CAS ]
  • [ 53518-18-6 ]
  • 4NO3(1-)*C16H14F3NO2*4C53H46N2O6*2Pt(2+) [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water-d2 at 20℃; for 1h;
  • 6
  • [ 53518-18-6 ]
  • [ 62-53-3 ]
  • C 153-aniline complex [ No CAS ]
YieldReaction ConditionsOperation in experiment
In cyclohexane
  • 7
  • C212H184N8O24Pt2(4+)*4NO3(1-) [ No CAS ]
  • [ 53518-18-6 ]
  • C212H184N8O24Pt2(4+)*4NO3(1-)*C16H14F3NO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water-d2 at 80℃; for 1h;
  • 8
  • 4C57H66N2O12*2Pt(2+)*4NO3(1-) [ No CAS ]
  • [ 53518-18-6 ]
  • 4C57H66N2O12*2Pt(2+)*4NO3(1-)*2C16H14F3NO2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
In water-d2 at 80℃; for 1h;
  • 9
  • [ 53518-18-6 ]
  • thione coumarin 153 [ No CAS ]
YieldReaction ConditionsOperation in experiment
66.54% With Lawessons reagent In toluene at 110℃; for 12h; Inert atmosphere; 1 Synthesis of 9-(trifluoromethyl)-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyrido[3,2,1-ij]quinoline -11-thione Under nitrogen protection, 2.00 g (6.47 mmol) of 9-(trifluoromethyl)-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyridine[3,2,1-ij]quinolin-11-one and Lawesson's reagent 3.92 g (9.72 mmol) 1:1.5 equivalent were added to 20 mL of dry re-distilled toluene, and stirred at 110 °C for 12 hours to obtain a red solution; Spin dry the red reaction solution in step a, recrystallize from ethyl acetate to obtain a red solid, namely 9-(trifluoromethyl)-2,3,6,7-tetrahydro-1H, 5H, 11H-pyrano [2,3-f]pyrido[3,2,1-ij]quinoline-11-thione 1.4 g yielded 66.54%.
  • 10
  • [ 53518-18-6 ]
  • (E)-2-(pyrimidin-4-yl)-2-(9-(trifluoromethyl)-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyridine[3,2,1-ij]quinoline-11-ethylene)acetonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: Lawessons reagent / toluene / 12 h / 110 °C / Inert atmosphere 2.1: sodium hydride / acetonitrile / 0.5 h / 20 °C / Inert atmosphere; Darkness 2.2: 2 h / 20 °C / Inert atmosphere; Darkness 2.3: 1.5 h / 20 °C / Inert atmosphere; Darkness
  • 11
  • [ 53518-18-6 ]
  • (E)-1-(4-boronaminobenzyl)-4-(cyano(9-(trifluoromethyl)-2.3.6.7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyrido[3,2,1-ij]quinoline-11-ylidene)methyl)pyrimidin-1-ammonium bromide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: Lawessons reagent / toluene / 12 h / 110 °C / Inert atmosphere 2.1: sodium hydride / acetonitrile / 0.5 h / 20 °C / Inert atmosphere; Darkness 2.2: 2 h / 20 °C / Inert atmosphere; Darkness 2.3: 1.5 h / 20 °C / Inert atmosphere; Darkness 3.1: acetonitrile / 12 h / 80 °C
  • 12
  • [ 53518-18-6 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: Lawessons reagent / toluene / 15 h / 100 °C / Inert atmosphere 2.1: sodium hydride / acetonitrile / 3 h 2.2: 2 h / 20 °C / Inert atmosphere
  • 13
  • [ 53518-18-6 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: Lawessons reagent / toluene / 15 h / 100 °C / Inert atmosphere 2.1: sodium hydride / acetonitrile / 3 h 2.2: 2 h / 20 °C / Inert atmosphere 3.1: dichloromethane / 16 h / 20 °C / Inert atmosphere
  • 14
  • [ 53518-18-6 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: Lawessons reagent / toluene / 15 h / 100 °C / Inert atmosphere 2.1: sodium hydride / acetonitrile / 3 h 2.2: 2 h / 20 °C / Inert atmosphere 3.1: acetonitrile; ethyl acetate / 48 h / 60 °C
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