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Chemical Structure| 1220039-64-4 Chemical Structure| 1220039-64-4

Structure of 1220039-64-4

Chemical Structure| 1220039-64-4

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Product Details of [ 1220039-64-4 ]

CAS No. :1220039-64-4
Formula : C4H4Br2N2
M.W : 239.90
SMILES Code : BrC1=CC=NN=C1.[H]Br
MDL No. :MFCD15474999
InChI Key :KSJDIQGRNABAMU-UHFFFAOYSA-N
Pubchem ID :53407906

Safety of [ 1220039-64-4 ]

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

Application In Synthesis of [ 1220039-64-4 ]

* 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 [ 1220039-64-4 ]

[ 1220039-64-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1220039-64-4 ]
  • [ 4522-35-4 ]
  • [ 1616069-42-1 ]
YieldReaction ConditionsOperation in experiment
To a solution of<strong>[4522-35-4]3-iodo-1H-pyrazole</strong> (0.75 g) in DMSO (19 mL), was added60% NaH (0.39 g) under ice cooling and stirred for 10 min. 4-bromopyridazinehydrobromide (1.4 g) was added and stirred at room temperature for 3 days.Then 60% NaH (0.16 g) was added at 0 OC and warmed to room temperatureand stirred for 1 day. The reaction mixture was diluted with water and EtOAc. The mixture was filtered with Celite, and extracted with EtOAc. The combinedorganic layer was washed with brine and dried with anhyd. Na2S04. It wasfiltered to remove insoluble matters and it was concentrated in vacuo. Theresidue was triturated (Hexane:EtOAc= 1:1) to obtain compound 2-1 as a brownsolid.
 

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