Phenylic alcohol

Synonym(s) Benzenol, hydroxybenzene, monophenol, oxybenzene, phenyl alcohol, phenyl hydrate, phenyl hydroxide, phenylic acid, phenylic alcohol Lewis 1996... 

Synonyms AI3-01814 AIDS-352 Baker s P and S liquid and ointment Benzenol BRN 0969616 Carbolic acid Carbolic oil Caswell No. 649 CCRIS 504 CRS EINECS 203-632-7 EPA pesticide chemical code 064001 FEMA No. 3223 Fenosmolin Fenosmoline Hydroxy-benzene IPH Izal Monohydroxybenzene Monophenol NA 2821 NCI-C50124 NSC 36808 Oxybenzene Phenic acid Phenic alcohol Phenol alcohol Phenyl hydrate Phenyl hydroxide Phenylic acid Phenylic alcohol RCRA waste number U188 UN 1671 UN 2312 UN 2821. 

Phenyl hydrate, see Phenol Phenyl hydride, see Benzene Phenyl hydroxide, see Phenol Phenylic acid, see Phenol Phenylic alcohol, see Phenol Phenylmethane, see Toluene Phenyl methanol, see Benzyl alcohol Phenyl methyl alcohol, see Benzyl alcohol iV-Phenylmethylamine, see Methylaniline... 

Aromatic alcohols are called phenols. The word phenol comes from phenyl alcohol. Phenol itself, formerly known as carbolic acid, finds application as a preservative. Three example phenols are illustrated in Figure 11.23. Hexachlo-rophene, a phenolic aryl halide, was once a common active ingredient in over-the-counter antibacterial soaps. 

Zeolite beta has also been used for the racemization of secondary phenylic alcohols in a dynamic kinetic resolution however, in this case water elimination/ addition via a carbenium ion is involved rather than a redox mechanism [75, 76]. 

Composition Contains the basic ingredients of rose oil geraniol, citronellol, nerol, phenyl alcohol, ethyl alcohol... 

Figure 22-12. Schematic illustrating likely n-n and dipole stacking interactions between the 3,5-dinitrophenyl carbamate derivative or iec-phenyl alcohol and the naphthyl carbamoylated P-CD stationary phase. (R = H or naphthylethyl carbamate). (Reprinted from reference 61, with permission.)...

SYNS ACIDE CARBOLIQUE (FRENCH) BAKER S P AND S LIQUID and OINTMENT BENZENOL CARBOLIC ACID CARBOLSAEURE (GERMAN) FENOL PUTCH, POLISH) FENOLO (ITALIAN) H T)ROXYBENZENE MONOHYDROXYBENZENE MONOPHENOL NCI-C50124 OXYBENZENE PHENIC ACID PHENOL, molten pOT) PHENOL ALCOHOL PHENOLE (GERMAN) PHENYL HYDRATE PHENYL HYDROXIDE PHENYLIC ACID PHENYLIC ALCOHOL RCRA WASTE NUMBER U188... 

A mixture of phenyl Grignard and zinc halide adds to aldehydes in the presence of a stoichiometric amount of (1 ,2S)-DBNE to afford optically active phenyl alcohols with 82% ee in 90% yield (eq 10). ... 

Carbolic acid hydroxybenzene oxybenzene phenic acid phenyl hydrate phenyl hydroxide phenylic acid phenylic alcohol. 

Phcnylsulfuric acid is monobasic like ethylsulfuric acid the rule leads to this conclusion if one considers carbolic acid [phenol] as neutral, as phenyl alcohol, if one assumes its basicity to be zero, as in alcohol. 

H.1) (H.l) Phenol, phenol, phenyl alcohol, phenic acid, benzenol, hydroxybenzene (108-95-21 FEMA 3223... 

Synonyms/Trade Names Carbolic acid, Hydroxybenzene, Monohydroxybenzene, Phenyl alcohol, Phenyl hydroxide ... 

Synonyms hydroxybenzene carbolic acid phenic acid phenyl hydroxide phenylic alcohol benzenol... 

CAS 108-95-2 EINECS/ELINCS 203-632-7 UN 1671 (solid) UN 2312 (fused) UN 2821 (sol n.) FEMA 3223 Synonyms Benzenol Carbolic acid Hydroxybenzene Liquid phenol Monohydroxybenzene Monophenol Oxybenzene Phenic acid Phenol alcohol Phenol, liquefied Phenyl hydrate Phenyl hydroxide Phe-nylic acid Phenylic alcohol... 

Phenyl 2-hydro]raphenyl ketone. See 2-Hydroxybenzophenone Phenylic acid Phenylic alcohol. See Phenol 2,2 -(Phenylimino) diethanol. See Phenyidiethanolamine Phenyl ketone. See Benzophenone Phenylmercuri acetate. See Phenylmercuric acetate... 

Monophenol Oxybenzene Phenic acid Phenol alcohol Phenol, liquefied Phenyl hydrate Phenyl hydroxide Phenylic acid Phenylic alcohol... 

Li, M., Yang, Z., Hao, J., Shan, L., Dong, J. (2008). Determination of tyrosol, 2-phenyl alcohol, and tryptophol in beer by high-performance liquid chromatography. Journal of the American Society of Brewing Chemists, 66,245-249. http //dx.doi.org/10.1094/ASBCJ-2008-0914-01. 

The retention characteristics of over 40 small polar molecules (phenols, phenyl alcohols, imines, phenylcarboxylic acids, phenyl esters, phenyl. ethers, phenyl ketones, nitro- and cyanophenols) were studied on C4 and C g stationary phases [117]. Experimental results explain the advantages of methanol over other organic mobile phase components (e.g., acetonitrile) in the separation of aliphatic alcohols, phenols, and carboxylic acids. Methanol, through its reciprocal hydrogen bond donor/acceptor character forms stable complexes with these solutes in the stationary phase, giving enhanced selectivity for these solute types. The k values for these 40 solutes are tabulated for 20/80, 25/75, and 50/50 methanol/water mobile phases. 

Forty percent of 2-phenyl alcohol was also obtained. 

To acetonitrile was added periodic acid and this mixture was stirred at r.t. for 15 min. Dichlorofluoromethyl 4-methoxy-phenyl alcohol was added followed by addition of pyridinium chlorochromate in acetonitrile, then the reaction mixture was stirred at 0°, for 10 min and at r.t. for 2.5 h (62%) [6087]. 

Alcohols are organic compounds that have a functional hydroxyl group attached to a carbon atom of an alkyl chain. Benzene hydroxyl derivatives and aromatic hydrocarbons are called phenols, and the hydroxyl group is directly attached to a carbon atom in the benzene ring. In this case, phenol is an alcohol but not an alkyl alcohol the group QH5- is named phenyl but the CsHsOH compound is called phenol and not phenylic alcohol. 

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