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272345

Sigma-Aldrich

2,4,6-Triphenylpyrylium tetrafluoroborate

98%

Synonym(s):

2,4,6-Triphenylpyrylium fluoborate (6CI), 2,4,6-Triphenylpyrylium fluoroborate, 2,4,6-Triphenylpyrylium tetrafluoroborate (7CI), TPPT

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About This Item

Empirical Formula (Hill Notation):
C23H17BF4O
CAS Number:
Molecular Weight:
396.19
Beilstein:
3586533
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

powder

reaction suitability

reaction type: Photocatalysis
reagent type: catalyst

mp

250-251 °C (lit.)

photocatalyst activation

462 nm

SMILES string

F[B-](F)(F)F.c1ccc(cc1)-c2cc([o+]c(c2)-c3ccccc3)-c4ccccc4

InChI

1S/C23H17O.BF4/c1-4-10-18(11-5-1)21-16-22(19-12-6-2-7-13-19)24-23(17-21)20-14-8-3-9-15-20;2-1(3,4)5/h1-17H;/q+1;-1

InChI key

VQYPWMWEJGDSTF-UHFFFAOYSA-N

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Application

2,4,6-Triphenylpyrylium tetrafluoroborate was used as a sensitizer to carry out the photooxidation of cathecol. It was also used in the preparation of three N-alkylpyridinium photosensitizers by reacting with (1R,2S)-(-)-norephedrine, (S)-(+)-2-(aminomethyl)pyrrolidine and (R)-(-)-1-cyclohexylethylamine.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Three N-alkylpyridinium photosensitizers having chiral alkyl groups have been prepared by reacting 2,4,6-triphenylpyrylium tetrafluoroborate ion with (1R,2S)-(-)-norephedrine, (S)-(+)-2-(aminomethyl)pyrrolidine, and (R)-(-)-1-cyclohexylethylamine. Laser flash photolysis allows detection of the corresponding triplet excited states that are quenched by hydrogen atom donors and electron
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A high-performance liquid chromatography method based on pre-column derivatization with the pyrylium salts (4-[p-(N,N-dimethylamino)phenyl]-2,6-diphenylpyrylium perchlorate (LN1) and 2,4,6-triphenylpyrylium tetrafluoroborate (L1)) has been developed for the determination of sulfide. After the reaction of sulfide ions with LN1 or L1 aiming at

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