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4.6- Dichloro-3-methylphenol

A/,A/-Dichloro-4-methylbenzenesulfonamide Dichloromethylborane 2,3-Dichloro-2-methylbutane 1,1-Dichloromethyl methyl ether 2.4-Dichloro-3-methylphenol 2.4-Dichloro-6-methylphenol... [Pg.297]

In contrast with the Schiff base salen, salicylaldehyde oxime (79) (salox) complexes of Co have received comparatively little attention, but a series of bis-bidentate divalent complexes of the form iraiis-Co(sa 1 ox)2( D M SO)2 have been reported.343 The heterocyclic bidentate oxime violurate (lH,3H-pyrimidine-2,4,5,6-tetrone 5-oximate, Hvi) (80) and its /V-methyl (mvi) and /V,/V -dimethyl (dmvi) derivatives form high-spin divalent [Co(vi)]+ and Co(vi)2 complexes, whereas [Co(vi)3] is low spin.344 The mixed-ligand Co(dmvi)2(phen) complex is also low spin. The crystal structure of m-Co(pxo)2Br2 (pxo = 2-acetylpyridine-l-oxide oxime) is isostructural with the Ni11 relative.345 The dichloro complex also adopts a cis configuration. The tridentate dioximes 2,6-diformyl-4-methylphenol dioxime and 2,6-diacetyl-4-methylphenol dioxime (Hdampo) form binuclear complexes of the type (81a) and (81b) respectively.346 Cobalt oxide nanoparticles were prepared by... [Pg.36]

Chloro-2,4-dinitrobenzene, 2091 4-Chloro-2,5 -diethoxynitrobenzene, 3295 4-Chloro-2-methylphenol, 2737 2-Chloro-5-nitrobenzenesulfonic acid, 2137 Chlorobenzene, 2221 f 2-Chlorofluorobenzene, 2127 f 3-Chlorofluorobenzene, 2128 f 4-Chlorofluorobenzene, 2129 2-Chloronitrobenzene, 2134 4-Chloronitrobenzene, 2135 4-Chlorotrifluoromethylbenzene, 2642 1,5-Dichloro-2,4-dinitrobenzene, 2070... [Pg.2369]

Trapido M, Veressinina Y, Munter R (1998) Advanced Oxidation Process for Degradation of 2,4-Dichloro- and 2,4-Di-methylphenol, J. Environ. Eng.124 690-694. [Pg.237]

C7H6BrN02 2-amino-5-bromobenzoic acid 5794-88-7 538.66 47.611 2 10267 C7H6CI20 2,4-dichloro-5-methylphenol 1124-07-8 507.15 44.572 1,2... [Pg.451]

C7H6BrN02 1 -bromo-2-methyl-3-nitrobenzene 55289-35-5 538.66 47.611 2 10269 C7H6CI20 2,6-dichloro-3-methylphenol 13481-70-4 510.15 44.860 1,2... [Pg.451]

Fig. 5-53. Separation of various mono- and polyvalent phenols. - Separator column Ion Pac NS1 (10 pm) eluent (A) 0.01 mol/L KH2P04 (pH 4.0) / acetonitrile (90 10 v/v), (B) 0.01 mol/L KH2P04 (pH 4.0) / acetonitrile (20 80 v/v) gradient linear, 15% B in 20 min to 55% B flow rate 1 mL/min detection UV (280 nm) injection volume 50 pL solute concentrations 100 ppm each of pyrogallic acid (1), resorcinol (2), phenol (3), o-cresol (4), 2,4-di-methylphenol (5), /J-naphthol (6), 2,4-dichloro-3-nitrophenol (7), and thymol (8). Fig. 5-53. Separation of various mono- and polyvalent phenols. - Separator column Ion Pac NS1 (10 pm) eluent (A) 0.01 mol/L KH2P04 (pH 4.0) / acetonitrile (90 10 v/v), (B) 0.01 mol/L KH2P04 (pH 4.0) / acetonitrile (20 80 v/v) gradient linear, 15% B in 20 min to 55% B flow rate 1 mL/min detection UV (280 nm) injection volume 50 pL solute concentrations 100 ppm each of pyrogallic acid (1), resorcinol (2), phenol (3), o-cresol (4), 2,4-di-methylphenol (5), /J-naphthol (6), 2,4-dichloro-3-nitrophenol (7), and thymol (8).
HYDROXYDE de SODIUM (French) (1310-73-2) A strong base. Reacts with water, evolving heat and corrosive fumes. Violent reaction with acids, halogenated hydrocarbons, nitrogen-containing compounds, organic halogens, 4-chloro-2-methylphenol, 2,2-dichloro-... [Pg.641]


See other pages where 4.6- Dichloro-3-methylphenol is mentioned: [Pg.451]    [Pg.279]    [Pg.271]    [Pg.258]    [Pg.307]    [Pg.308]    [Pg.295]    [Pg.306]    [Pg.952]    [Pg.968]    [Pg.178]    [Pg.1233]    [Pg.1233]    [Pg.586]    [Pg.630]    [Pg.630]    [Pg.175]    [Pg.176]    [Pg.176]    [Pg.401]    [Pg.285]    [Pg.301]    [Pg.188]    [Pg.229]    [Pg.229]    [Pg.451]    [Pg.451]    [Pg.199]    [Pg.499]    [Pg.274]    [Pg.318]    [Pg.586]    [Pg.223]    [Pg.956]    [Pg.958]    [Pg.272]    [Pg.624]    [Pg.716]    [Pg.840]    [Pg.1068]    [Pg.1077]    [Pg.1079]    [Pg.1080]    [Pg.1238]   
See also in sourсe #XX -- [ Pg.7 , Pg.96 ]




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