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Chemical Structure| 26254-35-3 Chemical Structure| 26254-35-3

Structure of 26254-35-3

Chemical Structure| 26254-35-3

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Product Details of [ 26254-35-3 ]

CAS No. :26254-35-3
Formula : C12H5BrO2
M.W : 261.07
SMILES Code : O=C1C(C2=C3C1=CC=CC3=C(C=C2)Br)=O
MDL No. :MFCD18448738
Boiling Point : No data available
InChI Key :PHPQHHFMRUWUJG-UHFFFAOYSA-N
Pubchem ID :11173024

Safety of [ 26254-35-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 26254-35-3 ]

* 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 [ 26254-35-3 ]

[ 26254-35-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 26254-35-3 ]
  • [ 619-60-3 ]
  • [ 1265828-89-4 ]
  • 2
  • [ 26254-35-3 ]
  • [ 613-73-0 ]
  • C22H9BrN2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With piperidine; at 0 - 20℃; for 73h; 100 mmol of 1,2-Phenylenediacetonitrile, 90 mmol of 5-Acenaphthenequinone, solvent piperidine were mixed and cooled to 0C, stirred for 1 hour, and then warmed to room temperature for 3 days. After completion of the reaction, an excess of 5% dilute hydrochloric acid was added and the mixture was filtered. The filter cake was collected, washed with deionized water and recrystallized from nitrobenzene. Filteration and filter cake eluted with isohexane to give 1-160 mmol of product
160 mmol With piperidine; at 0 - 20℃; for 72h; Step 1. 100mmol <strong>[613-73-0]1,2-benzenediacetonitrile</strong>, 90mmol acenaphthenequinone, piperidine mixed solvent cooled to 0 C, stirring for 1 hour, then warmed to room temperature for 3 days, after the completion of the reaction, adding an excess of 5% The dilute hydrochloric acid was filtered and the cake was collected, washed with deionized water and recrystallized from nitrobenzene. It is filtered and the filter cake is rinsed with isohexane to give 3 160 mmol of product.
 

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