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Chemical Structure| 341-02-6 Chemical Structure| 341-02-6

Structure of 341-02-6

Chemical Structure| 341-02-6

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Product Details of [ 341-02-6 ]

CAS No. :341-02-6
Formula : C19H15BF4
M.W : 330.13
SMILES Code : F[B-](F)(F)F.[C+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
MDL No. :MFCD00013120
InChI Key :VQXBOEYKSVVPSP-UHFFFAOYSA-N
Pubchem ID :2723955

Safety of [ 341-02-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P403+P233-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 341-02-6 ]

* 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 [ 341-02-6 ]

[ 341-02-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19955-99-8 ]
  • [ 341-02-6 ]
  • 3-(3,3-Diphenylindan-1-yl)benzaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
41% With benzophenone; triethylamine; In toluene; at 80℃; for 48h; General procedure: A round bottom flask equipped with a magnetic stir-bar was charged with styrene (1.0 mmol),benzophene (0.3 mmol), triethylamine (1.0 mmol) and toluene (2.5 mL). Aftrer sterring for 1.0min, triphenylcarbenium tetrafluoroborate (1.5 mmol) was added and the resulting mixture wasallowed to react at 80 C for 48 h . After the end of the reaction, the mixture was filteredthrough a plug of Celite and eluted with hexanes/EtOAc (8:2). The filtrate was concentrated invacuo and purified by column chromatography on silica gel.
 

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