Nitro phenyl toluidine

Cl 37100. See 2-Methyl-4-nitroaniline Cl 37105. See 2-Methyl-5-nitroaniline Cl 37107. See p-Toluidine Cl 37110. See 3-Nitro-p-toluidine Cl 37115. See o-Anisidine hydrochloride Cl 37130. See 2-Methoxy-5-nitroaniline Cl 37225. See Benzidine Cl 37230. See o-Tolidine Cl 37235. See Dianisidine Cl 37240. See N-Phenyl-p-phenylenediamine Cl 37500. See P-Naphthol Cl 40000. See Direct yellow 11 Cl 40002 Cl 40003. See 4,4 -Diaminostilbene-2,2 -disulfonic acid Cl 40645. See Sodium-2-(4-styrvl-3-sulfophenyl)-2H-naphtho-(1,2-d)-triazole Cl 40800... 

In this method the nitro group in the aliphatic nitro compound is usually present on a carbon atom, which is also activated by CO-functioiiality (aldehyde, ester, arylketoiie). A successful application of this method is the Borsche modification of the Friedlander synthesis, involving condensation of A-(3-amino-4-picolylidene)-p-toluidine (17) with [Pg.289]

Propanenitrile, 3-(ethyl(3-methylphenyl)amino)-. See N-Cyanoethyl-N-ethyl-m-toluidine Propanenitrile, 3-( ethyl phenyl amino)-. See Cyanoethylethyl aniline Propanenitrile, 2-hydroxy-2-methyl-. See 2-Hydroxy-2-methylpropanenitrile Propanenitrile, 3-methoxy-. See 3-Methoxypropionitrile Propane, 2-nitro-. See2-Nitropropane Propaneperoxoic acid, 2-methyl-, 1,1-dimethylethyl ester. Seet-Butyl peroxyisobutyrate... 

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