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Chemical Structure| 173443-43-1 Chemical Structure| 173443-43-1

Structure of 173443-43-1

Chemical Structure| 173443-43-1

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Product Details of [ 173443-43-1 ]

CAS No. :173443-43-1
Formula : C11H16IO3P
M.W : 354.12
SMILES Code : O=P(CC1=CC=C(I)C=C1)(OCC)OCC
MDL No. :MFCD09033365
InChI Key :ACYSYNIYTMHNSY-UHFFFAOYSA-N
Pubchem ID :15166405

Safety of [ 173443-43-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H412
Precautionary Statements:P273

Application In Synthesis of [ 173443-43-1 ]

* 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 [ 173443-43-1 ]

[ 173443-43-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 110677-45-7 ]
  • [ 173443-43-1 ]
  • [ 1395880-55-3 ]
  • 2
  • [ 110677-45-7 ]
  • [ 173443-43-1 ]
  • C26H18IN [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With potassium tert-butylate; at 0 - 20℃; for 0.5h; 4-oxazol benzaldehyde (516 mg, 2 mmol) andDiethyl-4-iodophenethyl phosphate (708 mg, 2 mmol) was dissolved in dry tetrahydrofuran (20 mL) and cooled to 0 C. Potassium tert-butoxide (267 mg, 2.4 mmol) was added to the solution several times with stirring. After the addition was completed, stirring was continued for 30 minutes at room temperature.After the end of the reaction, 20 ml of water was added to precipitate a solid precipitate. Filtration, the solid was washed with ethanol, and the crude product was crystallized from ethyl acetate. After drying, 753 mg of a pale yellow solid was obtained, yield 80%.
 

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