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Chemical Structure| 88738-86-7 Chemical Structure| 88738-86-7

Structure of 88738-86-7

Chemical Structure| 88738-86-7

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Product Details of [ 88738-86-7 ]

CAS No. :88738-86-7
Formula : C11H11BrO2
M.W : 255.11
SMILES Code : O=C(OC)/C=C/C1=CC=C(CBr)C=C1
MDL No. :MFCD02684186
InChI Key :ZSRCGGBALFGALF-VOTSOKGWSA-N
Pubchem ID :11658908

Safety of [ 88738-86-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 88738-86-7 ]

* 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 [ 88738-86-7 ]

[ 88738-86-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 88738-86-7 ]
  • [ 186590-01-2 ]
  • (E)-4-((2-cyano-5-fluorophenoxy)methyl)cinnamic acid methyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
87% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 3h; In a single-mouth round bottom flask,2-cyano-5-fluoro-phenol (0.68 g, 5 mmol) was dissolved in 25 ml of dry DMF.Potassium carbonate (1.38 g, 10 mmol) was added.Stir at room temperature and add (E)-4-bromomethyl benzoate (1.27 g, 5 mmol).Stirring reaction was continued for 3 h, and the reaction was complete by TLC.Quenched with water, extracted with ethyl acetate (3×30 mL).Dry over anhydrous sodium sulfate and remove the solvent under reduced pressure.Petroleum ether / dichloromethane = 1/2 elution,The white solid product was obtained in 1.36 g (yield: 87%).
  • 2
  • [ 72955-97-6 ]
  • [ 88738-86-7 ]
  • (E)-4-((2-methoxy-5-fluorophenoxy)methyl)cinnamic acid methyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
84% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; for 3h; In a one-neck round flask, 5-fluoro-2-methoxy - phenol (728mg, 5.13mmol) dissolved in 6ml of DMF dry,Potassium carbonate (1.42 g, 10.3 mmol) was added.Stir at room temperature and add (E)-4-bromomethyl benzoate (1.31 g, 5.13 mmol).Stirring reaction was continued for 3 h, and the reaction was complete by TLC.Quenched with water, extracted with ethyl acetate (3×30 mL).Dry over anhydrous sodium sulfate and remove the solvent under reduced pressure.Petroleum ether / dichloromethane = 1 / 1 elution,The product was obtained as a colorless oil, 1.36 g (yield 84%).
 

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