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[ CAS No. 139564-41-3 ] {[proInfo.proName]}

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Chemical Structure| 139564-41-3
Chemical Structure| 139564-41-3
Structure of 139564-41-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 139564-41-3 ]

CAS No. :139564-41-3 MDL No. :MFCD19220105
Formula : C7H13NO Boiling Point : -
Linear Structure Formula :- InChI Key :IASLVFGXHJQWAB-LURJTMIESA-N
M.W : 127.18 Pubchem ID :13082303
Synonyms :

Safety of [ 139564-41-3 ]

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 [ 139564-41-3 ]

* 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 [ 139564-41-3 ]

[ 139564-41-3 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 139564-39-9 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
81% With ammonia; sodium In tetrahydrofuran; ethanol -33 deg C to r.t., 4 h;
  • 2
  • [ 935658-79-0 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
70% Stage #1: (R,E)-dibenzyl 1-(6-ethoxy-2-methyl-6-oxohex-4-en-3-yl)hydrazine-1,2-dicarboxylate With hydrogen In methanol for 12h; Stage #2: In ethanol at 50℃; for 5h;
  • 3
  • [ 1064654-96-1 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: LiBr; DBU / acetonitrile / 0.75 h / 5 °C 2.1: H2 / Raney-Ni / methanol / 12 h / 3102.89 Torr 2.2: 70 percent / ethanol / 5 h / 50 °C
  • 4
  • [ 590-86-3 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: L-proline / acetonitrile / 3 h / 0 - 10 °C 2.1: LiBr; DBU / acetonitrile / 0.75 h / 5 °C 3.1: H2 / Raney-Ni / methanol / 12 h / 3102.89 Torr 3.2: 70 percent / ethanol / 5 h / 50 °C
  • 5
  • [ 41654-04-0 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: 84 percent / toluene / 18.5 h / Heating 2: 94 percent / Et3SiH, TiCl4 / CH2Cl2 / a) -78 deg C, 1.5 h, b) r.t., 12 h 3: 81 percent / Na, liq. NH3 / ethanol; tetrahydrofuran / -33 deg C to r.t., 4 h
Multi-step reaction with 4 steps 1.1: sulfuric acid / 20 °C 2.1: titanium(IV) tetraethanolate / 72 °C / Inert atmosphere 3.1: [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 2-Amino-2-methyl-1-propanol; potassium <i>tert</i>-butylate / isopropyl alcohol / 50 °C / Molecular sieve 4.1: hydrogenchloride / methanol / 20 °C 4.2: 0.17 h / pH > 11
  • 6
  • [ 137869-71-7 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 94 percent / Et3SiH, TiCl4 / CH2Cl2 / a) -78 deg C, 1.5 h, b) r.t., 12 h 2: 81 percent / Na, liq. NH3 / ethanol; tetrahydrofuran / -33 deg C to r.t., 4 h
  • 7
  • ethyl 4-[(S)-tert-butylsulfinylimino]-5-methylhexanoate [ No CAS ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 2-Amino-2-methyl-1-propanol; potassium <i>tert</i>-butylate / isopropyl alcohol / 50 °C / Molecular sieve 2.1: hydrogenchloride / methanol / 20 °C 2.2: 0.17 h / pH > 11
  • 8
  • [ 54857-48-6 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: titanium(IV) tetraethanolate / 72 °C / Inert atmosphere 2.1: [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; 2-Amino-2-methyl-1-propanol; potassium <i>tert</i>-butylate / isopropyl alcohol / 50 °C / Molecular sieve 3.1: hydrogenchloride / methanol / 20 °C 3.2: 0.17 h / pH > 11
  • 9
  • C13H27NO3S [ No CAS ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Stage #1: C13H27NO3S With hydrogenchloride In methanol at 20℃; Stage #2: With ammonia; ammonium chloride; sodium hydroxide In water for 0.166667h;
  • 10
  • [ 628-46-6 ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 20 °C 1.2: 20 °C 2.1: tetrahydrofuran / 20 °C 3.1: C47H47ClIrN3O5 / 12 h / 20 °C
  • 11
  • C7H15NO2 [ No CAS ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: tetrahydrofuran / 20 °C 2: C47H47ClIrN3O5 / 12 h / 20 °C
  • 12
  • [ 920-66-1 ]
  • C8H13NO3 [ No CAS ]
  • C10H15F6NO2 [ No CAS ]
  • [ 139564-41-3 ]
YieldReaction ConditionsOperation in experiment
1: 45% 2: 52% With C47H47ClIrN3O5 at 20℃; for 12h; enantioselective reaction;
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