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2-Methoxynitrobenzene

Methoxynaphthalene, AT21 ij.-Methoxy-2-ni troani I ine, AK56 2-Methoxynitrobenzene, AK34 3 Methoxynitrobenzene, AK35... [Pg.635]

SYNS l-METHOXY-2-NITROBENZENE 2-METHOXYNITROBENZENE NCI-C60388 2-NITROANISOLE o-NITROPHENYL METHYL ETHER... [Pg.1006]

Synonyms Anisole, o-nitro- Benzene, 1-methoxy-2-nitro- 1-Methoxy-2-nitrobenzene 2-Methoxynitrobenzene 2-Nitroanisole o-Nitrobenzene methyl ether o-Nitrophenyl methyl ether Empirical C7H7NO3 Formula CH3OC6H4NO2 Properties Lt. reddish or amber clear liq. sol. in DMSO, alcohol, 95% ethanol, acetone, ether sol. [Pg.2823]

Nitroanisole (4-methoxynitrobenzene) [100-17-4] M 153.1, m 54". Crystd from pet ether or hexane and dried in vacuo. [Pg.309]

Reduction of nitrobenzene (Grant Streitwieser 1978 Todres, Dyusengaliev et al. 1984) and 4-methoxynitrobenzene (Todres, Dyusengaliev et al. 1984) by uranium-, thorium-, and lanthanum-di(cyclooctatetraene) complexes leads to azo compounds. Scheme 1-17 illustrates these reductive reactions using uranium-(C8H8)2 complex as an example. [Pg.24]

The electronic properties of the nitroarene strongly influence the reactivity. Whereas nitrobenzene 38a gave the amination product 30a in high yield, electron-withdrawing substituents decreased the yield. With 4-methoxynitrobenzene 38d, almost no product 30d was isolated. [Pg.105]

Aminoethyl)aminoethanol, see A-2-Hydroxyethyl-1,2-diaminoethane, 1750 2-(2-Aminoethylamino)-5-methoxynitrobenzene, 3166... [Pg.2044]

The solvatochromic effects on UV/visible spectra of certain solutes are so large, that they can conveniently be employed as probes for certain solvating properties of the solvents. Those that have enjoyed widespread application in this capacity are discussed in Chapter 4. They include 2,6-diphenyl -4-(2,4,6-triphenyl-l-pyridino)-phenoxide, 4-methoxynitrobenzene, 4-(dimethylamino)-nitrobenzene, for the estimation of the polarity of solvents, acetylacetonato-N,N,N, N -tetramethylethylenediamino-copper(II) perchlorate, 4-nitrophenol, and 4-nitroaniline, for the estimation of the electron pair donicity of solvents, 4-carboxymethyl-l-ethylpyridinium iodide, 4-cyano-l-ethylpyridinium iodide, and bis-c/.v-1, lO-phenanthrolinodicyano-iron(II) for the estimation of the hydrogen bond donation abilities of solvents (Marcus 1993). [Pg.111]

SYNS 2-AMINO-1-METHOXY-4-NITROBENZENE 3-AiMINO-4-METHOXYNITROBENZENE 2-AMINO-4-NITROANISOLE o-ANISIDINE NITRATE AZOAMINE SCARLET AZOGENE ECARLATE R AZOIC DIAZO COMPONENT 13 BASE C.I. AZOIC DIAZO COMPONENT 13 C.I. 37130 FAST SCARLET R 2-METHOXY-5-NITROANILINE 2-METHOXY-5-NITROBENZENAMINE NCI-C01934 3-NTTRO-6-METHOXYANTLINE 5-NITRO-2-METHOXYANILINE... [Pg.1006]

SYNS p-METHOXYNITROBENZENE 1-METHOXY-4-NITROBENZENE 4-METHOXYNITROBENZENE p-NITROANISOL 4-NITROANISOLE... [Pg.1007]

METHOXYNITROBENZENE see NER500 p-METHOXYNITROBENZENE see NER500 1-METHOXY-2-NITROBENZENE see NEROOO... [Pg.1765]

Fig. 29.10 H-NMR spectra of (a) methylbenzene (b) methoxybenzene (c) nitrobenzene (d) 1,4-dimethylbenzene (e) 4-methoxynitrobenzene (f) 4-amino-3-bromonitrobenzene (NH2 protons not shown). Fig. 29.10 H-NMR spectra of (a) methylbenzene (b) methoxybenzene (c) nitrobenzene (d) 1,4-dimethylbenzene (e) 4-methoxynitrobenzene (f) 4-amino-3-bromonitrobenzene (NH2 protons not shown).
Dimethyl-5-methoxyindole prepared via the VNS cyanomethylation of 3-methyl-4-methoxynitrobenzene has been used as starting material for the synthesis of cyclopropano-annelated quinone methide, a reductive alkylating agent for in vitro studies of its interactions with deoxyguanosine-5 -monophosphate (Scheme 67) [185]. [Pg.84]

Amino-1 -methoxy-4-nitrobenzene 3-Amino-4-methoxynitrobenzene. See 2-Methoxy-5-nitroaniline... [Pg.229]


See other pages where 2-Methoxynitrobenzene is mentioned: [Pg.309]    [Pg.1765]    [Pg.309]    [Pg.560]    [Pg.858]    [Pg.948]    [Pg.316]    [Pg.358]    [Pg.358]    [Pg.2566]    [Pg.309]    [Pg.1046]    [Pg.5]    [Pg.272]    [Pg.253]    [Pg.262]    [Pg.262]    [Pg.635]    [Pg.1104]    [Pg.2465]    [Pg.1046]    [Pg.361]    [Pg.148]    [Pg.374]    [Pg.1508]    [Pg.1765]    [Pg.309]    [Pg.309]    [Pg.260]    [Pg.260]    [Pg.560]    [Pg.858]    [Pg.948]    [Pg.1046]    [Pg.1954]    [Pg.316]    [Pg.316]    [Pg.683]    [Pg.358]    [Pg.358]    [Pg.358]    [Pg.358]   
See also in sourсe #XX -- [ Pg.560 ]




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2-Nitroanisole, 2-Methoxynitrobenzene

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