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Chemical Structure| 1439-07-2 Chemical Structure| 1439-07-2

Structure of 1439-07-2

Chemical Structure| 1439-07-2

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Product Details of [ 1439-07-2 ]

CAS No. :1439-07-2
Formula : C14H12O
M.W : 196.24
SMILES Code : [C@@H]1(C2=CC=CC=C2)O[C@H]1C3=CC=CC=C3
MDL No. :MFCD00064311

Safety of [ 1439-07-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302+H312+H332-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P363-P403+P233-P405-P501

Application In Synthesis of [ 1439-07-2 ]

* 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 [ 1439-07-2 ]

[ 1439-07-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1095-03-0 ]
  • [ 1439-07-2 ]
  • (1RS,2RS)-2-phenoxy-1,2-diphenyl-1-ethanol [ No CAS ]
  • (1RS,2SR)-2-phenoxy-1,2-diphenyl-1-ethanol [ No CAS ]
  • 2
  • [ 5350-41-4 ]
  • [ 100-52-7 ]
  • [ 1689-71-0 ]
  • [ 1439-07-2 ]
YieldReaction ConditionsOperation in experiment
General procedure: Ammonium salt 6 (1 equiv.) was suspended in dry THF (0.05 M) andstirred at 40 °C. t-BuOK (4 equiv.) was added and the mixture was stirred vigorously. After 10 minutes 2 equiv. of aldehyde 2 were added and the mixture was stirred for 3 hours at 40 °C. The reaction was then quenched by addition of a half-saturated NaCl solution. After phase separation, the aqueous phase was extracted three times with DCM and the combined organic phases were dried with Na2SO4 and evaporated to dryness. Purification by columnchromatography (gradient of heptanes and EtOAc) gave the corresponding epoxides in the reported yields as a mixture of diastereomers.
 

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