54827-40-6

Basic information

• Product Name: 2,6-ditert-butyl-4-[4-(dimethylamino)phenyl]pyrylium
• Synonyms: 2,6-ditert-butyl-4-[4-(dimethylamino)phenyl]pyrylium
• CAS NO: 54827-40-6
• Molecular Formula: C21H30NO+
• Molecular Weight: 312.469
• Mol File: 54827-40-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-ditert-butyl-4-[4-(dimethylamino)phenyl]pyrylium(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-ditert-butyl-4-[4-(dimethylamino)phenyl]pyrylium(54827-40-6)
• EPA Substance Registry System: 2,6-ditert-butyl-4-[4-(dimethylamino)phenyl]pyrylium(54827-40-6)

Safety Data

• Hazardous Substances Data: 54827-40-6(Hazardous Substances Data)

Upstream product

• 3315-60-4 methanolate 
• 104241-55-6 [4-(2,6-Di-tert-butyl-2-methoxy-2H-pyran-4-yl)-phenyl]-dimethyl-amine 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 104241-55-6 [4-(2,6-Di-tert-butyl-2-methoxy-2H-pyran-4-yl)-phenyl]-dimethyl-amine 

Relevant articles and documents

Fast Atom Bombardment Mass Spectroscopy: a Useful Technique for Structural Characterization of Pyrylium, Thiopyrylium, and Pyridinium Cations

It is shown that fast atom bombardment (f.a.b.) mass spectrometry is well suited of the title compounds (thirty nine examples are given).Glycerol and bis-(2-hydroxyethyl) sulphide appear to be the best matrices.Spectra are characterized by large peaks cor

Quantitative Comparison of the Heteroatom Effects in the Methoxide Attachment to Pyrylium and Thiopyrylium Cations. Thermodynamics of the Isomerization of Pyrans and Thiopyrans

The complete set of kinetic and equilibrium constants for the methoxide attachment to a series of 2,6-di-tert-butyl-4-arylpyrylium cations (aryl = XC6H4 with X = p-NO2, m-Cl, p-Cl, H, p-Me, p-OMe, p-NMe2) has been obtained in MeOH at 25 deg C.These data complement those previously obtained by studying the methoxide attachment to the corresponding thiopyrylium cations.In both series the reaction involves the kinetically controlled formation of both the corresponding 2H and 4H adducts which equilibrate to form only the thermodynamically more stable 2 H adduct.The observed kinetic patterns show that the rate-determining step is the combination of the nucleophile with the cation to give the adducts.Moreover, the experimental data indicate that the Leffler-Hammond postulate cannot give information on the position of the transition state along the reaction coordinate.Both kinetic and equilibrium constants for the formation of the 2H and 4H adducts are correlated with the ?+ constants.The obtained ρ values show, for the pyrylium series, a greater sensitivity to the substituent effects with respect to the corresponding thiopyrylium series.From the equilibrium data we estimate that, in contrast with quantum mechanical calculations, the unsubstituted 2H-pyran is at least 4.6 kcal/mol more stable than the corresponding 4H isomer.