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[ CAS No. 509094-03-5 ] {[proInfo.proName]}

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Chemical Structure| 509094-03-5
Chemical Structure| 509094-03-5
Structure of 509094-03-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 509094-03-5 ]

CAS No. :509094-03-5 MDL No. :MFCD13248594
Formula : C13H16N2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 248.28 Pubchem ID :-
Synonyms :

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* 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 [ 509094-03-5 ]

[ 509094-03-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 114615-82-6 ]
  • [ 509094-02-4 ]
  • [ 70187-32-5 ]
  • [ 509094-03-5 ]
YieldReaction ConditionsOperation in experiment
In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 32.b Example 32 (b) To a solution of 4-cyclohexylamino-3-nitrobenzyl alcohol (21.0 g, 83 mmol) in DCM (300 mL) was added powdered 4 Å molecular sieves (15 g) and N-methyl morpholine-N-oxide monohydrate (10.8 g, 92.2 mmol). Tetra-n-propylammonium perruthenate (VII) (2.91 g, 8.28 mmol) was then added in a single portion. An initial exotherm was controlled using an ice bath, and then the reaction mixture was stirred at room temperature for 18 hr. The mixture was then reduced to ~100 mL by evaporation, and loaded onto a column of silica (400 g). The column was eluted with acetone:hexane 1:3 and the spot at 0.30 was collected, affording 4-cyclohexylamino-3-nitrobenzaldehyde as a yellow solid. (11.0 g, 44.3 mmol): 1H NMR (CDCl3, 300 MHz) δ9.60 (s, 1 H), 8.32 (s, 1 H), 7.71 (d, J=10 Hz,1 H), 6.73 (d, J=10 Hz, 1 H) 3.46-3.32 (m, 1 H), 1.90-1.15 (m, 10 H).
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