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[ CAS No. 1054451-31-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1054451-31-8
Chemical Structure| 1054451-31-8
Structure of 1054451-31-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1054451-31-8 ]

CAS No. :1054451-31-8 MDL No. :N/A
Formula : C26H22B2O4 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 420.07 Pubchem ID :-
Synonyms :

Safety of [ 1054451-31-8 ]

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

Application In Synthesis of [ 1054451-31-8 ]

* 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 [ 1054451-31-8 ]

[ 1054451-31-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1054451-31-8 ]
  • [ 474918-32-6 ]
  • [ 1601479-57-5 ]
YieldReaction ConditionsOperation in experiment
55% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 12h;Reflux; Inert atmosphere; General procedure: A mixture of 2 (0.83 g, 2.2 mmol), 5 (0.48 g, 1 mmol), Pd(PPh3)4 (0.11g, 0.1mmol), and K2CO3 (1.1 g, 8.0 mmol) in toluene/ethanol/water (100 mL, 8/1/1 v/v/v) was heated to reflux for 12 h under nitrogen. Then the reaction mixture was cooled to room temperature and poured into water. The organic layer was extracted with dichloromethane, and the combined organic layers were washed with a saturated brine solution and water, and dried over anhydrous magnesium sulfate. After filtration and solvent evaporation, the residue was purified by silica-gel column chromatography using hexane/dichloromethane as eluent. White solid of (TPE)2PF was obtained in 56% yield.
  • 2
  • [ 1054451-31-8 ]
  • [ 171408-76-7 ]
  • [ 1601479-58-6 ]
YieldReaction ConditionsOperation in experiment
45% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene for 12h; Reflux; Inert atmosphere; 2.3.1 9,9-Diphenyl-2,7-bis(4-(1,2,2-triphenylvinyl)phenyl)fluorene ((TPE)2PF) General procedure: A mixture of 2 (0.83 g, 2.2 mmol), 5 (0.48 g, 1 mmol), Pd(PPh3)4 (0.11g, 0.1mmol), and K2CO3 (1.1 g, 8.0 mmol) in toluene/ethanol/water (100 mL, 8/1/1 v/v/v) was heated to reflux for 12 h under nitrogen. Then the reaction mixture was cooled to room temperature and poured into water. The organic layer was extracted with dichloromethane, and the combined organic layers were washed with a saturated brine solution and water, and dried over anhydrous magnesium sulfate. After filtration and solvent evaporation, the residue was purified by silica-gel column chromatography using hexane/dichloromethane as eluent. White solid of (TPE)2PF was obtained in 56% yield.
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