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Chemical Structure| 17056-93-8 Chemical Structure| 17056-93-8

Structure of 17056-93-8

Chemical Structure| 17056-93-8

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Product Details of [ 17056-93-8 ]

CAS No. :17056-93-8
Formula : C12H10O2
M.W : 186.21
SMILES Code : CC(C1=C(O)C=C2C=CC=CC2=C1)=O
MDL No. :MFCD04339089

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Application In Synthesis of [ 17056-93-8 ]

* 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 [ 17056-93-8 ]

[ 17056-93-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17056-93-8 ]
  • [ 31680-08-7 ]
  • (2E)-1-(3-hydroxynaphthalen-2-yl)-3-(4-methoxy-3-nitrophenyl)prop-2-en-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In methanol; at 0 - 20℃; General procedure: To a stirred solution of the appropriate ketone (1 mM) and asubstituted aldehyde (1 mM) in 25 ml methanol, was addedpulverized NaOH (2 mM) and the mixture was stirred at roomtemperature for 24-36 h. The reaction was monitored by TLC usingn-hexane: ethyl acetate (7:3) as mobile phase. The reactionmixture was cooled to 0 C (ice-water bath) and acidified withHCl (10% v/v aqueous solution) to afford total precipitation of thecompounds. In most cases, a yellow precipitate was formed, whichwas filtered and washed with 10% aqueous HCl solution. In thecases where an orange oil was formed, the mixture was extractedwith CH2Cl2, the extracts were dried (Na2SO4) and the solvent wasevaporated to give the respective chalcone (1a-1f).
With sodium hydroxide; In methanol; General procedure: To a stirred solution of 2'-hydroxy-1'-acetonaphthone (1 mM)and a substituted aldehyde (1 mM) in 25 ml methanol, was added pulverized NaOH (2 mM) and the mixture was stirred at room temperature for 24-36 h. The reaction was monitored by TLC using n-hexane: ethyl acetate (7:3) as mobile phase. The reaction mixture was cooled to 0 C (ice-water bath) and acidified with HCl (10% v/v aqueous solution) to afford total precipitation of the compounds. In most cases, a yellow precipitate was formed, which was filtered and washed with 10% aqueous HCl solution. In the cases where an orange oil was formed, the mixture was extracted with CH2Cl2, the extracts were dried (Na2SO4) and the solvent was evaporated to give the respective chalcone (1a-5a).
 

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