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Methyl Phenylcarbinol

Figure 5. Experimental evidence of rate of entrainment by Tetralin in methyl-phenylcarbinol oxidation T = 60°C. Figure 5. Experimental evidence of rate of entrainment by Tetralin in methyl-phenylcarbinol oxidation T = 60°C.
Strong specific and non-specific interactions which produce labile diastereomeric solvates. In these solvates, each isomer is sufficiently different for some of the enantiomeric nuclei to be in magnetically different environments. Another nice example of the formation of NMR spectroscopically different diastereomeric solvates are solutions of (—)-cocaine in [K)- and (5 )-methyl phenylcarbinol [418]. [Pg.387]

Methyl benzyl alcohol. SeeCresyl alcohol o-Methylbenzyl alcohol CAS 98-85-1 EINECS/ELINCS 202-707-1 UN 2937 (DOT) FEMA 2685 Synonyms Benzenemethanol, a-methyl- Ethanol, 1-phenyl- Methyl phenylcarbinol Methylphenylmethanol a-Phenethyl alcohol s-Phenethyl alcohol 1-Phenylethanol a-Phenylethyl alcohol Phenylmethylcarbinol Styrallyl alcohol Styralyl alcohol Empirical CsHioO Formula C6H5CH(CH3)OH Properties Colorless liq. mild floral odor sol. in alcohol, glycerol, min. oil, oxygenated and hydrocarbon soivs. si. sol. in water m.w. 122.17 dens. 1.009-1.014 vapor pressure 0.1 mm (20 C) ... [Pg.2591]

CggHggNgO 4.4, 4"-Trianilino-3-methyl.tri> phenylcarbinol, Carbinolbaae dea Anilin> blaua Oder Spritblaus 18, 768,1301. [Pg.3115]

An intimate mixture of equimolar amounts of triacetic acid lactone and di-phenylcarbinol heated ca. 0.5 hr. at 150-160° in an oil bath -> 3-diphenylmethyl-4-hydroxy-6-methyl-2-pyrone. Y 67%. F. e. s. K.-H. Boltze and K. Heidenbluth,... [Pg.232]


See other pages where Methyl Phenylcarbinol is mentioned: [Pg.535]    [Pg.590]    [Pg.2674]    [Pg.399]    [Pg.535]    [Pg.590]    [Pg.2674]    [Pg.399]    [Pg.135]    [Pg.105]   
See also in sourсe #XX -- [ Pg.590 ]




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