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Chemical Structure| 7338-94-5 Chemical Structure| 7338-94-5

Structure of 7338-94-5

Chemical Structure| 7338-94-5

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Product Details of [ 7338-94-5 ]

CAS No. :7338-94-5
Formula : C15H10O
M.W : 206.24
SMILES Code : O=C(C1=CC=CC=C1)C#CC2=CC=CC=C2
MDL No. :MFCD00156767
InChI Key :YECVQOULKHBGEN-UHFFFAOYSA-N
Pubchem ID :97637

Safety of [ 7338-94-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 7338-94-5 ]

* 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 [ 7338-94-5 ]

[ 7338-94-5 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 20101-92-2 ]
  • [ 7338-94-5 ]
  • [ 95734-21-7 ]
  • 3
  • [ 6414-69-3 ]
  • [ 7338-94-5 ]
  • (Z)-6-Oxo-4,6-diphenyl-hex-4-enoic acid ethyl ester [ No CAS ]
  • ethyl (E)-6-oxo-4,6-diphenylhex-4-enoate [ No CAS ]
  • 4
  • [ 593-85-1 ]
  • [ 7338-94-5 ]
  • [ 40230-24-8 ]
  • 5
  • [ 68176-57-8 ]
  • [ 7338-94-5 ]
  • 6-tert-butyl-2,3-diphenylquinoxaline [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% 1,3-diphenyl-2-yn-1-one 0.5mmol, 4- tert-butyl-o-phenylenediamine 0.6mmol, 10mL of ethanol was added 2mL of the reaction tube, placed in an oil bath at 40°C , the reaction 24h ; distilled ethanol was added 1 mmol of sodium methoxide, dimethyl sulfoxide 5mL, placed in an oil bath at 40°C , the reaction 1h. Adding an appropriate amount of water or sodium chloride solution, the reaction was stopped, cooled to room temperature. The reaction solution was diluted with ethyl acetate, washed with water three times, the organic phase was dried over anhydrous Na2SO4, filtered, concentrated and purified by column chromatography to give the target product 131.8mg, 78percent yield.
  • 6
  • [ 1195-33-1 ]
  • [ 7338-94-5 ]
  • 2-((4-bromophenyl)sulfonyl)-3-phenyl-1H-inden-1-one [ No CAS ]
  • 7
  • [ 14019-62-6 ]
  • [ 7338-94-5 ]
  • isopropyl (Z)-(3-oxo-1,3-diphenylprop-1-en-1-yl)glycinate [ No CAS ]
  • 8
  • [ 61150-58-1 ]
  • [ 7338-94-5 ]
  • 8-fluoro-2,4-diphenylbenzo[b]oxepine-5-carbonitrile [ No CAS ]
  • 9
  • [ 61150-58-1 ]
  • [ 7338-94-5 ]
  • 7-fluoro-2,4-diphenylbenzofuro[2,3-b]pyridine [ No CAS ]
  • 10
  • [ 6563-13-9 ]
  • [ 7338-94-5 ]
  • (7-methoxy-2-phenylpyrrolo[1,2-a]quinoline-1,3-diyl)bis(phenylmethanone) [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With copper diacetate; at 100℃; for 12h;Sealed tube; Add 0.2mmol 6-methoxyquinoline nitrogen oxide,0.5mmol of 1,3-diphenylprop-2-yn-1-one and 0.2eq Cu(OAc)2 are dissolved in a pressure tube containing 1.6mL PEG-200 (equipped with a magnetic stirrer), sealed and pressure resistant After the reaction was completed, it was extracted three times with 30 mL of ethyl acetate and saturated aqueous ammonium chloride solution. The organic phases were combined, dried with anhydrous MgSO4, concentrated, and separated by silica gel column chromatography to obtain 69 mg of yellow The solid compound, the yield is 72%,
 

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