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[ CAS No. 179898-27-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 179898-27-2
Chemical Structure| 179898-27-2
Structure of 179898-27-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 179898-27-2 ]

CAS No. :179898-27-2 MDL No. :MFCD05663966
Formula : C12H18N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 222.28 Pubchem ID :-
Synonyms :

Safety of [ 179898-27-2 ]

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

Application In Synthesis of [ 179898-27-2 ]

* 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 [ 179898-27-2 ]

[ 179898-27-2 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 67-64-1 ]
  • [ 179898-27-2 ]
  • [ 179898-28-3 ]
YieldReaction ConditionsOperation in experiment
With 4-tert-Butylcatechol; iodine; magnesium sulfate for 8h; Heating;
  • 2
  • [ 179898-26-1 ]
  • [ 179898-27-2 ]
YieldReaction ConditionsOperation in experiment
With hydrogen In ethanol; ethyl acetate for 6h; Ambient temperature;
  • 3
  • [ 24424-99-5 ]
  • [ 179898-27-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 4-(N,N-dimethylamino)pyridine / tetrahydrofuran / Ambient temperature 2: H2 / 10percent Pd/C / ethyl acetate; ethanol / 6 h / Ambient temperature
  • 4
  • [ 603-83-8 ]
  • [ 179898-27-2 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 4-(N,N-dimethylamino)pyridine / tetrahydrofuran / Ambient temperature 2: H2 / 10percent Pd/C / ethyl acetate; ethanol / 6 h / Ambient temperature
  • 5
  • [ 179898-27-2 ]
  • [ 179898-29-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature
  • 6
  • [ 179898-27-2 ]
  • [ 199609-67-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature
  • 7
  • [ 179898-27-2 ]
  • [ 179898-63-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h
  • 8
  • [ 179898-27-2 ]
  • [ 179897-36-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature 4: 44 percent / ZnCl2 / ethanol / 3 h / Heating
Multi-step reaction with 5 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature 4: ZnCl2 / ethanol / 3 h / Heating 5: 57percent aq. HI / 3 h / 60 °C
  • 9
  • [ 179898-27-2 ]
  • 1,6,8,8,10-Pentamethyl-4-trifluoromethyl-6,7,8,9-tetrahydro-1H-pyrido[3,2-g]quinolin-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature 4: 44 percent / ZnCl2 / ethanol / 3 h / Heating 5: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, RT, 4 h
Multi-step reaction with 6 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature 4: ZnCl2 / ethanol / 3 h / Heating 5: 57percent aq. HI / 3 h / 60 °C 6: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, RT, 4 h
  • 10
  • [ 179898-27-2 ]
  • 8-Ethoxy-2,2,4,10-tetramethyl-6-trifluoromethyl-1,2,3,4-tetrahydro-pyrido[3,2-g]quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: H2 / 10percent Pd/C / ethanol; ethyl acetate / 6 h 3: TFA / CH2Cl2 / 3 h / Ambient temperature 4: ZnCl2 / ethanol / 3 h / Heating
  • 11
  • [ 179898-27-2 ]
  • [ 179895-87-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature 3: 47 percent / ZnCl2 / ethanol / 3 h / Heating
Multi-step reaction with 4 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature 3: ZnCl2 / ethanol / 3 h / Heating 4: 57percent aq. HI / 3 h / 60 °C
  • 12
  • [ 179898-27-2 ]
  • 1,6,8,8,10-Pentamethyl-4-trifluoromethyl-8,9-dihydro-1H-pyrido[3,2-g]quinolin-2-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature 3: 47 percent / ZnCl2 / ethanol / 3 h / Heating 4: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, RT, 4 h
Multi-step reaction with 5 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature 3: ZnCl2 / ethanol / 3 h / Heating 4: 57percent aq. HI / 3 h / 60 °C 5: 1.) NaH / 1.) THF, 0 deg C, 30 min, 2.) THF, RT, 4 h
  • 13
  • [ 179898-27-2 ]
  • 8-Ethoxy-2,2,4,10-tetramethyl-6-trifluoromethyl-1,2-dihydro-pyrido[3,2-g]quinoline [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: MgSO4, 4-tert-butylcatechol, I2 / 8 h / Heating 2: TFA / CH2Cl2 / 3 h / Ambient temperature 3: ZnCl2 / ethanol / 3 h / Heating
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