phenyl


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Related to phenyl: phenylalanine

phenyl

phenyl (fĕnˈəl), C6H5, organic free radical or alkyl group derived from benzene by removing one hydrogen atom.
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phenyl

[′fen·əl]
(organic chemistry)
C6H5‒ A functional group consisting of a benzene ring from which a hydrogen has been removed.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.

phenyl

of, containing, or consisting of the monovalent group C6H5, derived from benzene
Collins Discovery Encyclopedia, 1st edition © HarperCollins Publishers 2005
References in periodicals archive ?
134-135[degrees]C; IR (KBr, [cm.sup.-1]): 3142 (N-H), 1716 (ring C=O), 1658 (C=O); [.sup.1]H-NMR (500 MHz, DMSO-[d.sub.6]): [delta] 10.72; 10.55 (2s, 1H, NH), 8.28; 8.20 (2s, 1H, imidazothiazole [C.sub.5]-H), 7.78 (d, 2H, J=8.78 Hz, 4-Brphenyl [C.sub.2,6]-H), 7.59 (d, 2H, J=8.30 Hz, 4-Brphenyl [C.sub.3,5]-H), 7.28-7.23 (m, 2H, phenyl), 7.21-7.16 (m, 3H, phenyl), 7.08; 7.05 (2s, 1H, imidazothiazole [C.sub.2]-H), 4.08-3.82 (m, 6H, C[H.sub.2]CO, SC[H.sub.2] and NC[H.sub.2]), 2.89 (t, 2H, J=7.32 Hz, C[H.sub.2]-Ph).
Reaction mechanism of cationic micellar catalysis upon the hydrolysis of mono-p-methoxy phenyl phosphate ester.
The contribution of C--O--C was positive to the photoelastic birefringence; however, the positive contribution of the phenyl ring was higher than that of C--O--C, leading to a high positive photoelastic birefringence for PPhMA, because the polarizability anisotropy of the phenyl ring (reported in Ref.
Togo, "Efficient demethylation of N,N-dimethylanilines with phenyl chloroformate in ionic liquids," Synlett, no.
Synthesis of N,N-Bis(4-(2-bromo-9-phenyl-fluoren-9-yl) phenyl)-4-(9-phenyl-2-(pyren-1-yl)-fluoren-9-yl)aniline.
A mixture of [5-oxo-4-(phenyl hydrazono)-3-trichloromethyl-4,5-dihydro-pyrazol1yl]-acetic acid hydrazide (5) (0.01 M), potassium thiocyanate (0.02 M), concentrated hydrochloric acid (1mL), ethanol (10mL) and water (20 mL) were refluxed for 3 h.
Mesamoll II alkylsulfonic phenyl ester from Lanxess Corp., Pittsburgh, can now be used in toys and food packaging.
(Atlanta, GA) have patented asymmetric derivatives of furamidines with one of the phenyl rings of furamidine replaced with a benzimidazole, found by quantitative footprinting analyses to bind GC containing sites on DNA more strongly than to pure AT sequences.