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[ CAS No. 51407-46-6 ] {[proInfo.proName]}

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Chemical Structure| 51407-46-6
Chemical Structure| 51407-46-6
Structure of 51407-46-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 51407-46-6 ]

CAS No. :51407-46-6 MDL No. :MFCD01940896
Formula : C13H18O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 190.28 Pubchem ID :-
Synonyms :

Safety of [ 51407-46-6 ]

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 [ 51407-46-6 ]

* 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 [ 51407-46-6 ]

[ 51407-46-6 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 51407-46-6 ]
  • [ 38861-78-8 ]
  • [ 15687-27-1 ]
  • [ 40150-92-3 ]
  • [ 105899-75-0 ]
YieldReaction ConditionsOperation in experiment
1: 85 % Chromat. 2: 7 % Chromat. 3: 2 % Chromat. 4: 1 % Chromat. With oxygen; manganese(II) stearate; 3-chloro-benzenecarboperoxoic acid In decane at 0℃; for 2h; other reagents and solvents, var. temperature, var. pressures;
  • 2
  • [ 36039-36-8 ]
  • [ 51407-46-6 ]
YieldReaction ConditionsOperation in experiment
91% With Dess-Martin periodane In dichloromethane Inert atmosphere;
80% With oxalyl dichloride; dimethyl sulfoxide; triethylamine In dichloromethane at -78℃;
74% With Dess-Martin periodane In dichloromethane at 20℃; for 1h; Inert atmosphere;
54% With oxalyl dichloride; dimethyl sulfoxide In dichloromethane at -78℃; for 1h;
With oxalyl dichloride; dimethyl sulfoxide; triethylamine 1) -65 deg C, CH2Cl2, 5 min; Multistep reaction;
327 mg With pyridinium chlorochromate In dichloromethane for 1.5h; Inert atmosphere; Schlenk technique;

  • 3
  • [ 51407-46-6 ]
  • [ 51146-56-6 ]
  • [ 51146-57-7 ]
  • 4
  • [ 41283-72-1 ]
  • [ 51407-46-6 ]
  • [ 36039-36-8 ]
YieldReaction ConditionsOperation in experiment
1: 65% 2: 15% With diisobutylaluminium hydride In diethyl ether; hexane at -78℃;
1: 65% 2: 15% With diisobutylaluminium hydride In diethyl ether; hexane at -78℃;
  • 5
  • [ 51523-49-0 ]
  • [ 51407-46-6 ]
  • [ 60601-66-3 ]
YieldReaction ConditionsOperation in experiment
In ethanol 1 EXAMPLE 1 EXAMPLE 1 α-(4-Isobutylphenyl)propionaldehyde (8.6 g., 0.045 mole) and 8.4 g. (0.045 mole) of 2-cyclohexylmethylpiperidine were dissolved in 200 ml. of absolute ethanol in a Parr hydro-generator and the mixture reduced with hydrogen over 703 mg. of palladium-on-charcoal. Reduction was complete in about 15 hours, and the mixture was filtered and the filtrate evaporated to dryness to give 16.3 g. of crude product which was chromatographed on 300 g. of alumina using 10% ether/90% hexane as eluent. There was thus obtained 10.0 g. of 2-cyclohexylmethyl-1-[2-(4-isobutylphenyl)propyl]piperidine as a colorless oil. The hydrochloride salt melts at 132° - 160°C.
  • 6
  • [ 36039-36-8 ]
  • [ 38861-78-8 ]
  • [ 51407-46-6 ]
  • [ 15687-27-1 ]
YieldReaction ConditionsOperation in experiment
1: 15% 2: 15% 3: 44% With sodium tungstate; dihydrogen peroxide; tetra(n-butyl)ammonium hydrogensulfate at 90℃;
  • 7
  • [ 51407-46-6 ]
  • [ 51146-56-6 ]
  • [ 51146-57-7 ]
  • [ 114937-30-3 ]
  • 8
  • [ 623-53-0 ]
  • [ 38861-78-8 ]
  • [ 51407-46-6 ]
  • 9
  • [ 51407-46-6 ]
  • [ 64758-90-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: diethyl ether / 3 h / 0 - 20 °C / Inert atmosphere 2: pyridinium chlorochromate; mesoporous silica / dichloromethane / 3 h / 20 °C / Inert atmosphere
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