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580-34-7

580-34-7 Structure

580-34-7 Structure
IdentificationBack Directory
[Name]

2,4,6-Tris(4-methoxyphenyl)pyrylium tetrafluoroborate
[CAS]

580-34-7
[Synonyms]

2,4,6-Tris(4-methoxyphenyl)pyrylium tetrafluoroborate
2,4,6-Tris(4-methoxyphenyl)pyrylium tetrafluoroborate >=95%
[Molecular Formula]

C26H23BF4O4
[MDL Number]

MFCD00160229
[MOL File]

580-34-7.mol
[Molecular Weight]

486.263
Chemical PropertiesBack Directory
[Melting point ]

346-351°C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

powder
[Appearance]

Orange to red Solid
[InChI]

1S/C26H23O4.BF3.FH/c1-27-22-10-4-18(5-11-22)21-16-25(19-6-12-23(28-2)13-7-19)30-26(17-21)20-8-14-24(29-3)15-9-20;2-1(3)4;/h4-17H,1-3H3;;1H/q+1;;/p-1
[InChIKey]

BYUPZXIJGVBLGP-UHFFFAOYSA-M
[SMILES]

COC(C=C1)=CC=C1C2=[O+]C(C3=CC=C(OC)C=C3)=CC(C4=CC=C(OC)C=C4)=C2.FB(F)F.[F-]
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

2,4,6-Tris(4-methoxyphenyl)pyrylium tetrafluoroborate can be used to catalyze the stereoselective synthesis of C2-symmetric cyclobutane alkene dimers via photo-induced electron transfer. This method can be employed for the total synthesis of lignans such as magnosalin, endiandrin A and pellucidin A. It can also catalyze photoinduced electron transfer (PET) to initiate radical-cation Diels-Alder reactions.
[reaction suitability]

reagent type: catalyst
reaction type: Photocatalysis
Spectrum DetailBack Directory
[Spectrum Detail]

2,4,6-Tris(4-methoxyphenyl)pyrylium tetrafluoroborate(580-34-7)1HNMR
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