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Phenol, p- 2- -ethyl

C8H10O p-ethyl phenol 123-07-9 in benzene 1.781 1 15431 C8H180 2-octanol 123-96-6 in benzene 1.649 1... [Pg.678]

Ethyl phenol. See p-Ethyl phenol m-Ethylphenol. See 3-Ethylphenol p-Ethylphenol... [Pg.1769]

Propyl succinate ( Ci qHi g0l4. ) + CarvacroK Ci oHmO) p-Ethyl- phenol ( CgHj qO ) 218.8 38 226.3... [Pg.621]

Preparation by reaction of benzoyl chloride with p-ethyl-phenol in the presence of aluminium chloride in tetra-chloroethane at 105° for 22 h (60%) [92]. [Pg.91]

Phenol with smaUer amounts of p-cresol, p-ethyl phenol, p-isopropyl- 201 phenyl phenol, bisphenol A, diphenyl ether, p-tolyl phenyl ether, p-ethyl diphenyl ether, p-isopropenyl diphenyl ether, isomers of lolyl (ethyl-phenyl)ether... [Pg.503]

McNeill and Rincon studied thermal degradation of PC by means of TGA, TVA, DSC, FT-IR, mass spectrometry (MS) and gas chromatogra-phy-MS (GC-MS) method (see Fig. 2.5). PC is stable up to 300°C. Above that temperature, small quantities of phenol and p-cresol were detected, at 375-400°C CO2 appeared and then at T > 455°C CO and CH4 were formed the peak on the DTG curve was at F = 462°C. At 500°C the main products are q chc dimer and bisphenol A, with small quantities of CO2, p-cresol, p-ethyl phenol, phenol, p-vinyl phenol, p-isopropyl phenol, CO and CH4. In the absence of air and moisture, degradation of PC proceeds by hemolytic decomposition of the polymer chain, radical reactions, fragmentations and molecular rearrangements. [Pg.35]


See other pages where Phenol, p- 2- -ethyl is mentioned: [Pg.342]    [Pg.223]    [Pg.439]    [Pg.38]    [Pg.345]    [Pg.584]    [Pg.183]    [Pg.145]    [Pg.66]    [Pg.266]    [Pg.6755]    [Pg.508]    [Pg.352]    [Pg.441]    [Pg.441]    [Pg.441]    [Pg.443]    [Pg.623]    [Pg.623]    [Pg.801]    [Pg.1040]    [Pg.39]    [Pg.7]    [Pg.410]    [Pg.263]    [Pg.125]    [Pg.299]    [Pg.1774]   
See also in sourсe #XX -- [ Pg.183 ]




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3- Ethyl phenol

P- phenol

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