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[ CAS No. 1009-27-4 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1009-27-4
Chemical Structure| 1009-27-4
Chemical Structure| 1009-27-4
Structure of 1009-27-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1009-27-4 ]

CAS No. :1009-27-4 MDL No. :MFCD13178666
Formula : C10H11NO Boiling Point : -
Linear Structure Formula :- InChI Key :LKEJIEFLJHCIAK-UHFFFAOYSA-N
M.W : 161.20 Pubchem ID :12287052
Synonyms :

Safety of [ 1009-27-4 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1009-27-4 ]

* 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 [ 1009-27-4 ]

[ 1009-27-4 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 108-31-6 ]
  • [ 1009-27-4 ]
  • [ 13191-50-9 ]
YieldReaction ConditionsOperation in experiment
In 1,4-dioxane Heating;
  • 2
  • [ 2085-31-6 ]
  • [ 1009-27-4 ]
  • [ 61579-91-7 ]
YieldReaction ConditionsOperation in experiment
In xylene for 0.2h; Heating;
YieldReaction ConditionsOperation in experiment
Rk. in festem od. geloestem Zustand m. Sauerstoff -> Indirubin;
Rk. m. CH3-O-C(O)-C-=C-C(O)-O-CH3 in abs. Dioxan <Dampfbad> -> /BRN= 488355/, /BRN= 488354/, /BRN= 492085/;
Rk. m. Tetrahydrofuran-boran -> Indol u. Indolin;
Rk. m. I2, Methanol-H2SO4 -> Isoindigo;
Rk. m. 1) Luft-O2, 2) HCl -> Indirubin;
Rk. m. 1) PbO2, 2) HCl -> Indirubin;
Rk. mit CH3-O2C-C-=C-CO2-CH3, abs. Dioxan, Dampfbad -> 1 (/BRN= 488355/), 2 (/BRN= 488354/), 3 (/BRN= 492085/);
Rk. mit THF-boran -> Indol u. Indolin;
fester oder geloester Zustand, Sauerstoffzutritt -> indirubin;
Rk. m. Piperidin, 24 h, Kochen, N2 -> 2-Piperidino-3H-indol;

YieldReaction ConditionsOperation in experiment
Oxindol + Triaethyloxonium-borfluorid;
(yield)90percent;
Oxindol, Triethyloxonium-borfluorid;
  • 5
  • [ 1009-27-4 ]
  • [ 14185-81-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: dioxane / Heating 2: Py
  • 6
  • [ 59-48-3 ]
  • [ 368-39-8 ]
  • [ 1009-27-4 ]
YieldReaction ConditionsOperation in experiment
Stage #1: 2-oxoindole; triethyloxonium fluoroborate Stage #2: With potassium carbonate
Stage #1: 2-oxoindole; triethyloxonium fluoroborate In chloroform at 0 - 20℃; for 16h; Stage #2: With tert-butyl methyl ether; triethylamine In chloroform; water at 20℃; for 0.5h;
  • 7
  • [ 1009-27-4 ]
  • [ 4006-43-3 ]
YieldReaction ConditionsOperation in experiment
30% In nitromethane at 195℃;
  • 8
  • [ 1009-27-4 ]
  • [ 109-77-3 ]
  • [ 156774-76-4 ]
YieldReaction ConditionsOperation in experiment
77% In nitromethane at 100 - 110℃;
  • 9
  • [ 1009-27-4 ]
  • benzyl 2'-ethoxy-5-methyl-6-phenylspiro[cyclohexane-1,3'-indol]-3-en-2-yl-carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: N,N,N',N'-tetramethylguanidine / water / 24 h / 20 °C / Darkness 2: C44H37O4P / dichloromethane / 48 h / 0 °C / Inert atmosphere
  • 10
  • [ 1009-27-4 ]
  • benzyl ((1S,2S,5R,6R)-2'-ethoxy-5-methyl-6-phenyl-spiro[cyclohexane-1,3'-indol]-3-en-2-yl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: N,N,N',N'-tetramethylguanidine / water / 24 h / 20 °C / Darkness 2: C48H37O4P / dichloromethane / 48 h / 0 °C / Inert atmosphere
  • 11
  • [ 100-52-7 ]
  • [ 1009-27-4 ]
  • 3-(4-bromobenzylidene)-2-ethoxy-3H-indole [ No CAS ]
  • 3-(4-bromobenzylidene)-2-ethoxy-3H-indole [ No CAS ]
YieldReaction ConditionsOperation in experiment
63.636 % de With N,N,N',N'-tetramethylguanidine In water at 20℃; for 24h; Darkness; Overall yield = 596 mg;
  • 12
  • [ 100-52-7 ]
  • [ 1009-27-4 ]
  • 3-benzylidene-2-ethoxy-3H-indole [ No CAS ]
YieldReaction ConditionsOperation in experiment
192 mg With N,N,N',N'-tetramethylguanidine In water at 20℃; for 24h; Darkness;
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