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Chemical Structure| 54446-36-5 Chemical Structure| 54446-36-5

Structure of 54446-36-5

Chemical Structure| 54446-36-5

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Product Details of [ 54446-36-5 ]

CAS No. :54446-36-5
Formula : C12H10BrN
M.W : 248.12
SMILES Code : BrC1=CC=C(C=C1)NC2=CC=CC=C2
MDL No. :MFCD07779504
InChI Key :CCIVUDMVXNBUCY-UHFFFAOYSA-N
Pubchem ID :6425786

Safety of [ 54446-36-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H315-H318-H335-H411
Precautionary Statements:P261-P273-P280-P305+P351+P338
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 54446-36-5 ]

* 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 [ 54446-36-5 ]

[ 54446-36-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 108-86-1 ]
  • [ 621-38-5 ]
  • [ 54446-36-5 ]
  • 2
  • [ 54446-36-5 ]
  • [ 17024-12-3 ]
  • [ 690658-63-0 ]
YieldReaction ConditionsOperation in experiment
With sodium t-butanolate;bis-triphenylphosphine-palladium(II) chloride; In xylene; at 130℃; for 12h; Mixed under argon flow were 73 g of 4-bromodiphenylamine (A4), 135 g of <strong>[17024-12-3]9-iodophenanthrene</strong>, 34 g of sodium t-butoxide (manufactured by Tokyo Kasei Kogyo Co., Ltd.), 4 g of bis(triphenylphosphine)palladium dichloride (manufactured by Tokyo Kasei Kogyo Co., Ltd.) and 1.5 liter of xylene, and they were reacted at 130C for 12 hours. Water was added to the reaction liquid, and the mixture was filtered through celite, followed by carrying out separation thereof with toluene. The oil layer was concentrated under reduced pressure to obtain crystal. This was refined through a column and then dissolved in toluene, and hexane was added thereto to reprecipitate crystal. It was filtered and then dried to obtain 82 g of N-(4-bromophenyl)-N-phenyl-9-aminophenanthrene (B3).
 

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